Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; The Mammography Quality Standards Act Requirements, 33811-33814 [2010-14317]

Download as PDF Federal Register / Vol. 75, No. 114 / Tuesday, June 15, 2010 / Notices FEDERAL RETIREMENT THRIFT INVESTMENT BOARD Sunshine Act; Notice of Meeting TIME AND DATE: 10 a.m. (Eastern Time), June 21, 2010. PLACE: 4th Floor Conference Room, 1250 H Street, NW., Washington, DC 20005. STATUS: Open to the public. MATTERS TO BE CONSIDERED: 1. Approval of the minutes of the May 17, 2010 Board member meeting. 2. Thrift Savings Plan activity report by the Executive Director. a. Monthly Participant Activity Report. b. Monthly Investment Performance Review. c. Legislative Report. CONTACT PERSON FOR MORE INFORMATION: Thomas J. Trabucco, Director, Office of External Affairs, (202) 942–1640. Dated: June 11, 2010. Megan G. Grumbine, Secretary (Acting), Federal Retirement Thrift Investment Board. [FR Doc. 2010–14523 Filed 6–11–10; 4:15 pm] BILLING CODE 6760–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the National Coordinator for Health Information Technology; HIT Policy Committee’s Privacy & Security Tiger Team Meeting; Notice of Meeting AGENCY: Office of the National Coordinator for Health Information Technology, HHS. ACTION: Notice of meeting. mstockstill on DSKH9S0YB1PROD with NOTICES This notice announces a forthcoming subcommittee meeting of a Federal advisory committee of the Office of the National Coordinator for Health Information Technology (ONC). The meeting will be open to the public. Name of Committee: HIT Policy Committee’s Privacy & Security Tiger Team. General Function of the Committee: To provide recommendations to the National Coordinator on a policy framework for the development and adoption of a nationwide health information technology infrastructure that permits the electronic exchange and use of health information as is consistent with the Federal Health IT Strategic Plan and that includes recommendations on the areas in which standards, implementation specifications, and certification criteria are needed. Date and Time: The meeting will be held on June 29, 2010, from 8 a.m. to 5:15 p.m./ Eastern Time. Location: Grand Hyatt Washington Hotel, 1000 H Street, NW., Washington, DC 20001 VerDate Mar<15>2010 17:15 Jun 14, 2010 Jkt 220001 (telephone: 202–582–1234). Please check the ONC Web site, https://healthit.hhs.gov, for additional information as it becomes available, instructions on how to listen via telephone or Web, and viewing a video recording of the event which will be available following the meeting. Contact Person: Judy Sparrow, Office of the National Coordinator, HHS, 330 C Street, SW., Washington, DC 20201, 202–205–4528, Fax: 202–690–6079, e-mail: judy.sparrow@hhs.gov. Please call the contact person for up-to-date information on this meeting. A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Agenda: The workgroup will be discussing technologies that enable consumer choice for sharing their information in health information exchange. The workgroup will be hearing testimony from current users of such technologies, developers of ‘‘cutting edge’’ technologies that may be useful in the clinical care setting in the future, as well as stakeholder groups. ONC intends to make background material available to the public no later than two (2) business days prior to the meeting. If ONC is unable to post the background material on its Web site prior to the meeting, it will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on ONC’s Web site after the meeting, at https://healthit.hhs.gov. Procedure: Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Written submissions may be made to the contact person on or before June 23, 2010. Oral comments from the public will be scheduled between approximately 5 p.m. and 5:15 p.m./Eastern Time. Time allotted for each presentation will be limited to three minutes. If the number of speakers requesting to comment is greater than can be reasonably accommodated during the scheduled open public hearing session, ONC will take written comments after the meeting until close of business on that day. Persons attending advisory committee meetings are advised that the agency is not responsible for providing access to electrical outlets. ONC welcomes the attendance of the public at its advisory committee meetings. Web registration is highly recommended and is available at https://www.blsmeetings.net/ consumerchoicetechnologyhearing. Seating is limited at the location, and ONC will make every effort to accommodate persons with physical disabilities or special needs. If you require special accommodations due to a disability, please contact Judy Sparrow at least seven (7) days in advance of the meeting. ONC is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at https://healthit.hhs.gov for procedures on public conduct during advisory committee meetings. Notice of this meeting is given under the Federal Advisory Committee Act (Pub. L. 92– 463, 5 U.S.C., App. 2). PO 00000 Frm 00053 Fmt 4703 Sfmt 4703 33811 Dated: June 9, 2010. Judith Sparrow, Office of Programs and Policy, Office of the National Coordinator for Health Information Technology. [FR Doc. 2010–14395 Filed 6–14–10; 8:45 am] BILLING CODE 4150–45–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2010–N–0121] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; The Mammography Quality Standards Act Requirements AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. DATES: Fax written comments on the collection of information by July 15, 2010. ADDRESSES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202–395–7285, or e-mailed to oira_submission@omb.eop.gov. All comments should be identified with the OMB control number 0910–0309. Also include the FDA docket number found in brackets in the heading of this document. FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of Information Management, Food and Drug Administration, 1350 Piccard Dr., PI50– 400B, Rockville, MD 20850, 301–796– 5156, Daniel.Gittleson@fda.hhs.gov. SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. The Mammography Quality Standards Act Requirements—21 CFR Part 900 (OMB Control Number 0910–0309)— Extension The Mammography Quality Standards Act requires the establishment of a Federal certification and inspection program for mammography facilities; E:\FR\FM\15JNN1.SGM 15JNN1 33812 Federal Register / Vol. 75, No. 114 / Tuesday, June 15, 2010 / Notices regulations and standards for accreditation and certification bodies for mammography facilities; and standards for mammography equipment, personnel, and practices, including quality assurance. The intent of these regulations is to assure safe, reliable, and accurate mammography on a nationwide level. Under the regulations, as a first step in becoming certified, mammography facilities must become accredited by an FDA-approved accreditation body. This requires undergoing a review of their clinical images and providing the accreditation body with information showing that they meet the equipment, personnel, quality assurance and quality control standards, and have a medical reporting and recordkeeping program, a medical outcomes audit program, and a consumer compliant mechanism. On the basis of this accreditation, facilities are then certified by FDA or an FDA approved State certification agency and must prominently display their certificate. These actions are taken to ensure safe, accurate, and reliable mammography on a nationwide basis. The following sections of title 21 of the Code of Federal Regulations (CFR) were not included in the previously mentioned burden tables because they were considered usual and customary practice and were part of the standard of care prior to the implementation of the regulations. Therefore, they resulted in no additional reporting or recordkeeping burden: 21 CFR 900.12(c)(1) and (c)(3) and 21 CFR 900.3(f)(1). Section 900.3(c) was not included in the previously mentioned burden tables because all four existing accreditation bodies are approved until late in 2013; so, no applicants will reapply during the requested information collection period. Section 900.24(c) was also not included in the previously mentioned burden tables because if a certifying state had its approval withdrawn, FDA would take over certifying authority for the affected facilities. Because FDA already has all the certifying state’s electronic records, there wouldn’t be an additional reporting burden. In the Federal Register of March 11, 2010 (75 FR 11542), FDA published a 60-day notice requesting public comment on the proposed collection of information. No comments were received. FDA estimates the burden of this collection of information as follows: TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN No. of Respondents Annual Frequency per Response 900.3(b)(1) 0.33 1 0.33 1 900.3(b)(3) full1 0.33 1 0.33 320 106 900.3(b)(3) limited2 5 1 5 30 150 900.3(c)3 1.33 1 1.33 15 20 900.3(d)(2) 0.1 1 0.1 30 3 900.3(d)(5) 0.1 1 0.1 30 3 900.3(e) 0.1 1 0.1 1 900.3(f)(2) 0.1 1 0.1 200 21 CFR Section 900.4(c), 900.11(b)(1), and 900.11(b)(2) facility4 Total Hours Total Operating & Maintenance Costs 20 2,894 1 5 2,894 1 2,894 5 1 5 211 8,681 1 8,681 1 8,681 5 1 5 1,736 8,680 $45 1,055 900.4(e) AB5 17:15 Jun 14, 2010 Jkt 220001 PO 00000 Frm 00054 Fmt 4703 1.5 $10,000 0.1 1 900.4(d) AB5 900.4(e), 900.11(b)(1), and 900.11(b)(2) facility4 Total Capital Costs 0.33 5 900.4(d), 900.11(b)(1), and 900.11(b)(2) facility4 mstockstill on DSKH9S0YB1PROD with NOTICES Hours per Response 2,894 900.4(c) AB5 VerDate Mar<15>2010 Total Annual Responses 421 2,105 .75 Sfmt 4703 4,341 $173,620 2,171 E:\FR\FM\15JNN1.SGM 15JNN1 $8,681 33813 Federal Register / Vol. 75, No. 114 / Tuesday, June 15, 2010 / Notices TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN—Continued 21 CFR Section No. of Respondents Annual Frequency per Response Total Annual Responses Hours per Response Total Hours Total Capital Costs Total Operating & Maintenance Costs 900.4(f) 331 1 331 7 2,317 $77,640 900.4(h) facility4 8,681 1 8,681 1 8,681 $3,820 900.4(h) AB5 5 1 5 10 50 900.4(i)(2) 1 1 1 16 16 900.6(c)(1) 0.1 1 0.1 60 6 900.11(b)(3) 5 1 5 400 1 400 8,681 4,942 42,901,502 87 1 87 900.12(h)(4) 7 1 7 1 7 900.12(j)(1) facility4 8 1 8 200 1,600 $120 900.12(j)(1) AB5 8 1 8 320 2,560 $240 900.12(j)(2) 2 1 2 100 200 $3,875 900.15(c) 5 1 5 2 10 900.15(d)(3)(ii) 1 1 1 2 2 900.18(c) 2 1 2 2 4 900.18(e) 2 1 2 1 2 900.21(b) 0.33 1 0.33 320 106 900.21(c)(2) 0.1 1 0.1 30 3 900.22(h) 5 200 1,000 900.22(i) 2 1 2 30 60 900.23 5 1 5 20 100 900.24(a) 0.4 1 0.4 200 80 $42 900.24(a)(2) 0.15 1 0.15 100 15 $21 900.24(b) 1 1 1 30 30 900.24(b)(1) 0.3 1 0.3 200 60 $42 900.24(b)(3) 0.15 1 0.15 100 15 $21 900.25(a) 0.2 1 0.2 16 900.11(c) 900.12(c)(2) 900.12(c)(2) patient refusal6 mstockstill on DSKH9S0YB1PROD with NOTICES FDA Form 3422 700 1 .5 5 .0833333 2.5 2,000 3,575,124 .5 43.5 .083 700 $30,000 $174 83 $20 3.2 .25 Total $19,500,000 175 3,620,692 1 One-time $40,000 $19,768,361 burden. 2 Refers to accreditation bodies applying to accredit specific Full Field Digital Mammography units. 3 While not included in the 60-day notice, all 4 accreditation bodies are expected to reapply to continue to be accreditation bodies during the information collection period. 4 Refers to the facility component of the burden for this requirement. 5 Refers to the accreditation body component of the burden for this requirement. 6 Refers to the situation where a patient specifically does not want to receive the lay summary of her exam. VerDate Mar<15>2010 17:15 Jun 14, 2010 Jkt 220001 PO 00000 Frm 00055 Fmt 4703 Sfmt 4703 E:\FR\FM\15JNN1.SGM 15JNN1 33814 Federal Register / Vol. 75, No. 114 / Tuesday, June 15, 2010 / Notices TABLE 2—ESTIMATED ANNUAL RECORDKEEPING BURDEN No. of Recordkeepers Annual Frequency per Recordkeeping Total Annual Records 900.3(f)(1) 0.1 1 0.1 0 0 900.4(g) 5 1 5 1 5 87 1 87 8 696 900.12(a)(4) 8,681 4 34,724 1 34,724 900.12(c)(4) 8,681 1 8,681 1 8,681 900.12(e)(13) 8,681 52 451,412 900.12(f) 8,681 1 8,681 16 138,896 900.12(h)(2) 8,681 2 17,362 1 17,362 900.22(a) 5 1 5 1 5 900.22(d) 5 1 5 1 5 900.22(e) 5 1 5 1 5 900.22(f) 3 1 3 1 3 900.22(g) 5 1 5 1 5 900.25(b) 5 1 5 1 5 21 CFR Section 900.12(a)(1)(i)(B)(2) Hours per Record .083333 Total [FR Doc. 2010–14317 Filed 6–14–10; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2010–N–0001] Tobacco Product Constituents Subcommittee of the Tobacco Products Scientific Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. mstockstill on DSKH9S0YB1PROD with NOTICES Notice. This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public. Name of Committee: Tobacco Product Constituents Subcommittee of the Tobacco Products Scientific Advisory Committee. General Function of the Committee: To provide advice and recommendations to the agency on FDA’s regulatory issues. VerDate Mar<15>2010 17:15 Jun 14, 2010 Jkt 220001 Date and Time: The meeting will be held on July 7, 2010, from 8:30 a.m. to 5 p.m. and on July 8, 2010, from 8 a.m. to 5 p.m. Location: Hilton Washington DC North/Gaithersburg, Montgomery Ballroom, 620 Perry Pkwy., Gaithersburg, MD 20877. The hotel phone number is 301–977–8900. Contact Person: Karen TempletonSomers, Office of Science, Center for Tobacco Products, Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 1–877–287–1373 (choose Option 4), e-mail: TPSAC@fda.hhs.gov or FDA Advisory Committee Information Line, 1–800– 741–8138 (301–443–0572 in the Washington, DC area), code 8732110002. Please call the Information Line for up-to-date information on this meeting. A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the agency’s Web site and call the appropriate advisory committee hot line/phone line to learn about possible modifications before coming to the meeting. Agenda: On July 7 and 8, 2010, the subcommittee will continue discussions, as needed, from the June 8 PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 Total Capital Costs Total Operating & Maintenance Costs $28,000 37,618 238,010 Dated: May 27, 2010. Leslie Kux, Acting Assistant Commissioner for Policy. ACTION: Total Hours $50 $28,000 $50 and 9, 2010, meeting of this subcommittee. The subcommittee will then receive presentations and discuss the analytic methods and ancillary and normalization standards applicable to the measurement and reporting of harmful or potentially harmful constituents in tobacco products, including smoke constituents. The subcommittee will finalize its proposed list of harmful or potentially harmful constituents, the rational for inclusion of each substance, validated methods for measuring the constituents and the ancillary and normalization standards for the identified constituents for presentation at a future meeting of the Tobacco Products Scientific Advisory Committee. FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s Web site after the meeting. Background material is available at https://www.fda.gov/ AdvisoryCommittees/Calendar/ default.htm. Scroll down to the appropriate advisory committee link. E:\FR\FM\15JNN1.SGM 15JNN1

Agencies

[Federal Register Volume 75, Number 114 (Tuesday, June 15, 2010)]
[Notices]
[Pages 33811-33814]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-14317]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2010-N-0121]


Agency Information Collection Activities; Submission for Office 
of Management and Budget Review; Comment Request; The Mammography 
Quality Standards Act Requirements

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
proposed collection of information has been submitted to the Office of 
Management and Budget (OMB) for review and clearance under the 
Paperwork Reduction Act of 1995.

DATES: Fax written comments on the collection of information by July 
15, 2010.

ADDRESSES: To ensure that comments on the information collection are 
received, OMB recommends that written comments be faxed to the Office 
of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, 
FAX: 202-395-7285, or e-mailed to oira_submission@omb.eop.gov. All 
comments should be identified with the OMB control number 0910-0309. 
Also include the FDA docket number found in brackets in the heading of 
this document.

FOR FURTHER INFORMATION CONTACT: Daniel Gittleson, Office of 
Information Management, Food and Drug Administration, 1350 Piccard Dr., 
PI50-400B, Rockville, MD 20850, 301-796-5156, 
Daniel.Gittleson@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, FDA has 
submitted the following proposed collection of information to OMB for 
review and clearance.

The Mammography Quality Standards Act Requirements--21 CFR Part 900 
(OMB Control Number 0910-0309)--Extension

    The Mammography Quality Standards Act requires the establishment of 
a Federal certification and inspection program for mammography 
facilities;

[[Page 33812]]

regulations and standards for accreditation and certification bodies 
for mammography facilities; and standards for mammography equipment, 
personnel, and practices, including quality assurance. The intent of 
these regulations is to assure safe, reliable, and accurate mammography 
on a nationwide level. Under the regulations, as a first step in 
becoming certified, mammography facilities must become accredited by an 
FDA-approved accreditation body. This requires undergoing a review of 
their clinical images and providing the accreditation body with 
information showing that they meet the equipment, personnel, quality 
assurance and quality control standards, and have a medical reporting 
and recordkeeping program, a medical outcomes audit program, and a 
consumer compliant mechanism. On the basis of this accreditation, 
facilities are then certified by FDA or an FDA approved State 
certification agency and must prominently display their certificate. 
These actions are taken to ensure safe, accurate, and reliable 
mammography on a nationwide basis. The following sections of title 21 
of the Code of Federal Regulations (CFR) were not included in the 
previously mentioned burden tables because they were considered usual 
and customary practice and were part of the standard of care prior to 
the implementation of the regulations. Therefore, they resulted in no 
additional reporting or recordkeeping burden: 21 CFR 900.12(c)(1) and 
(c)(3) and 21 CFR 900.3(f)(1). Section 900.3(c) was not included in the 
previously mentioned burden tables because all four existing 
accreditation bodies are approved until late in 2013; so, no applicants 
will reapply during the requested information collection period. 
Section 900.24(c) was also not included in the previously mentioned 
burden tables because if a certifying state had its approval withdrawn, 
FDA would take over certifying authority for the affected facilities. 
Because FDA already has all the certifying state's electronic records, 
there wouldn't be an additional reporting burden.
    In the Federal Register of March 11, 2010 (75 FR 11542), FDA 
published a 60-day notice requesting public comment on the proposed 
collection of information. No comments were received.
    FDA estimates the burden of this collection of information as 
follows:

                                                       Table 1--Estimated Annual Reporting Burden
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                Annual                                                          Total    Total Operating
              21 CFR  Section                   No.  of      Frequency per   Total Annual      Hours per       Total Hours     Capital     & Maintenance
                                              Respondents      Response       Responses        Response                         Costs         Costs
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(b)(1)                                           0.33               1           0.33         1                    0.33  ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(b)(3)                                           0.33               1           0.33       320                  106        $10,000  ...............
full\1\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(b)(3)                                           5                  1           5           30                  150     ..........  ...............
limited\2\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(c)\3\                                           1.33               1           1.33        15                   20     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(d)(2)                                           0.1                1           0.1         30                    3     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(d)(5)                                           0.1                1           0.1         30                    3     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(e)                                              0.1                1           0.1          1                    0.1   ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(f)(2)                                           0.1                1           0.1        200                   20     ..........              $45
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(c), 900.11(b)(1), and 900.11(b)(2)          2,894                  1       2,894            1.5              4,341     ..........  ...............
 facility\4\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(c)                                              5                  1           5          421                2,105     ..........         $173,620
AB\5\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(d), 900.11(b)(1), and 900.11(b)(2)          2,894                  1       2,894             .75             2,171     ..........  ...............
 facility\4\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(d)                                              5                  1           5          211                1,055     ..........  ...............
AB\5\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(e), 900.11(b)(1), and 900.11(b)(2)          8,681                  1       8,681            1                8,681     ..........           $8,681
 facility\4\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(e)                                              5                  1           5        1,736                8,680     ..........  ...............
AB\5\
--------------------------------------------------------------------------------------------------------------------------------------------------------

[[Page 33813]]

 
900.4(f)                                            331                  1         331            7                2,317     ..........          $77,640
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(h)                                          8,681                  1       8,681            1                8,681     ..........           $3,820
facility\4\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(h)                                              5                  1           5           10                   50     ..........  ...............
AB\5\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(i)(2)                                           1                  1           1           16                   16     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.6(c)(1)                                           0.1                1           0.1         60                    6     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.11(b)(3)                                          5                  1           5             .5                  2.5   ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.11(c)                                           400                  1         400            5                2,000     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(c)(2)                                      8,681              4,942  42,901,502             .0833333    3,575,124     ..........      $19,500,000
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(c)(2)                                         87                  1          87             .5                 43.5   ..........  ...............
patient refusal\6\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(h)(4)                                          7                  1           7            1                    7     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(j)(1)                                          8                  1           8          200                1,600     ..........             $120
facility\4\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(j)(1)                                          8                  1           8          320                2,560     ..........             $240
AB\5\
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(j)(2)                                          2                  1           2          100                  200     ..........           $3,875
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.15(c)                                             5                  1           5            2                   10     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.15(d)(3)(ii)                                      1                  1           1            2                    2     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.18(c)                                             2                  1           2            2                    4     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.18(e)                                             2                  1           2            1                    2     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.21(b)                                             0.33               1           0.33       320                  106        $30,000             $174
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.21(c)(2)                                          0.1                1           0.1         30                    3     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(h)                                             5                200       1,000             .083               83     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(i)                                             2                  1           2           30                   60     ..........              $20
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.23                                                5                  1           5           20                  100     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.24(a)                                             0.4                1           0.4        200                   80     ..........              $42
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.24(a)(2)                                          0.15               1           0.15       100                   15     ..........              $21
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.24(b)                                             1                  1           1           30                   30     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.24(b)(1)                                          0.3                1           0.3        200                   60     ..........              $42
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.24(b)(3)                                          0.15               1           0.15       100                   15     ..........              $21
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.25(a)                                             0.2                1           0.2         16                    3.2   ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
FDA Form 3422                                       700                  1         700             .25               175     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total                                                                                                          3,620,692        $40,000     $19,768,361
--------------------------------------------------------------------------------------------------------------------------------------------------------
\1\ One-time burden.
\2\ Refers to accreditation bodies applying to accredit specific Full Field Digital Mammography units.
\3\ While not included in the 60-day notice, all 4 accreditation bodies are expected to reapply to continue to be accreditation bodies during the
  information collection period.
\4\ Refers to the facility component of the burden for this requirement.
\5\ Refers to the accreditation body component of the burden for this requirement.
\6\ Refers to the situation where a patient specifically does not want to receive the lay summary of her exam.


[[Page 33814]]


                                                     Table 2--Estimated Annual Recordkeeping Burden
--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                  Annual                                                        Total    Total Operating
               21 CFR  Section                    No. of       Frequency per   Total Annual      Hours per      Total Hours    Capital     & Maintenance
                                               Recordkeepers   Recordkeeping     Records          Record                        Costs         Costs
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.3(f)(1)                                             0.1                1           0.1          0                  0     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.4(g)                                                5                  1           5            1                  5     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(a)(1)(i)(B)(2)                                  87                  1          87            8                696     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(a)(4)                                        8,681                  4      34,724            1             34,724     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(c)(4)                                        8,681                  1       8,681            1              8,681        $28,000  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(e)(13)                                       8,681                 52     451,412             .083333      37,618     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(f)                                           8,681                  1       8,681           16            138,896     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.12(h)(2)                                        8,681                  2      17,362            1             17,362     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(a)                                               5                  1           5            1                  5     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(d)                                               5                  1           5            1                  5     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(e)                                               5                  1           5            1                  5     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(f)                                               3                  1           3            1                  3     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.22(g)                                               5                  1           5            1                  5     ..........              $50
--------------------------------------------------------------------------------------------------------------------------------------------------------
900.25(b)                                               5                  1           5            1                  5     ..........  ...............
--------------------------------------------------------------------------------------------------------------------------------------------------------
Total                                                                                                            238,010        $28,000              $50
--------------------------------------------------------------------------------------------------------------------------------------------------------


    Dated: May 27, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010-14317 Filed 6-14-10; 8:45 am]
BILLING CODE 4160-01-S
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