Medical Diagnostic Equipment Accessibility Standards, 14706-14707 [2012-5964]

Download as PDF 14706 Federal Register / Vol. 77, No. 49 / Tuesday, March 13, 2012 / Proposed Rules U.S.C. 272 note) directs agencies to use voluntary consensus standards in their regulatory activities unless the agency provides Congress, through the Office of Management and Budget, with an explanation of why using these standards would be inconsistent with applicable law or otherwise impractical. Voluntary consensus standards are technical standards (e.g., specifications of materials, performance, design, or operation; test methods; sampling procedures; and related management systems practices) that are developed or adopted by voluntary consensus standards bodies. This proposed rule does not use technical standards. Therefore, we did not consider the use of voluntary consensus standards. Environment We have analyzed this proposed rule under Department of Homeland Security Management Directive 023–01 and Commandant Instruction M16475.lD, which guide the Coast Guard in complying with the National Environmental Policy Act of 1969 (NEPA) (42 U.S.C. 4321–4370f), and have made a preliminary determination that this action is one of a category of actions that do not individually or cumulatively have a significant effect on the human environment. A preliminary environmental analysis checklist Number supporting this determination is available in the docket where indicated under ADDRESSES. This proposed rule involves implementation of regulations at 33 CFR Part 165 that establish safety zones on navigable waters of the United States for fireworks events. These safety zones are enforced for the duration of fireworks display events. The fireworks are launched from or immediately adjacent to navigable waters of the United States and may have potential for negative impact on the safety or other interest of waterway users and near shore activities in the event area. The category of activities includes fireworks launched from barges at or near the shoreline that generally rely on the use of navigable waters as a safety buffer. This proposed rule is categorically excluded, under figure 2–1, paragraph (34)(g), of this instruction. This rule establishes a temporary safety zone to protect the public from fireworks fallout. An environmental analysis checklist and a preliminary categorical exclusion determination are available in the docket where indicated under ADDRESSES. We seek any comments or information that may lead to the discovery of a significant environmental impact from this proposed rule. requirements, Security measures, and Waterways. For the reasons discussed in the preamble, the Coast Guard proposes to amend 33 CFR part 165 as follows: List of Subjects in 33 CFR Part 165 Harbors, Marine safety, Navigation (water), Reporting and recordkeeping § 165.506 Safety Zones; Fifth Coast Guard District Fireworks Displays. Date PART 165—REGULATED NAVIGATION AREAS AND LIMITED ACCESS AREAS 1. The authority citation for part 165 continues to read as follows: Authority: 33 U.S.C. 1231; 46 U.S.C. Chapter 701, 3306, 3703; 50 U.S.C. 191, 195; 33 CFR 1.05–1, 6.04–1, 6.04–6, 160.5; Pub. L. 107–295, 116 Stat. 2064; Department of Homeland Security Delegation No. 0170.1. 2. § 165.506, in the Table to § 165.506, make the following amendments: a. Under ‘‘(d) Coast Guard Sector North Carolina-COTP Zone,’’ suspend entry 7, which will be enforced from June 7, 2012 through June 9, 2012, and from July 3, 2012 through July 8, 2012. b. Under ‘‘(d) Coast Guard Sector North Carolina-COTP Zone,’’ add entry 14 from June 7, 2012 through July 8, 2012, which will be enforced from 7:30 p.m. to 10 p.m. on June 8, 2012 and from 7:30 p.m. to 10 p.m. on July 4, 2012, to read as follows: * * Location * * * Regulated Area (d.) Coast Guard Sector North Carolina—COTP Zone * 14 ........ * * * * June 8, 2012, July 4, 2012 ........... * * * Dated: February 20, 2012. Anthony Popiel, Captain, U.S. Coast Guard, Captain of the Port North Carolina. [FR Doc. 2012–5493 Filed 3–12–12; 8:45 am] * * Pamlico River and Tar River, Washington, NC, Safety Zone. ARCHITECTURAL AND TRANSPORTATION BARRIERS COMPLIANCE BOARD 36 CFR Part 1195 [Docket No. ATBCB–2012–0003] BILLING CODE 9110–04–P emcdonald on DSK29S0YB1PROD with PROPOSALS RIN 3014–AA40 Medical Diagnostic Equipment Accessibility Standards Architectural and Transportation Barriers Compliance Board. ACTION: Notice of Intent to establish advisory committee. AGENCY: VerDate Mar<15>2010 14:04 Mar 12, 2012 Jkt 226001 PO 00000 Frm 00007 Fmt 4702 Sfmt 4702 * * All waters of Pamlico River and Tar River within a 300 yard radius of latitude 35°32′25″ N, longitude 077°03′42″ W, a position located on the southwest shore of the Pamlico River, Washington, NC. The Architectural and Transportation Barriers Compliance Board (Access Board) announces its intent to establish an advisory committee to advise the Board on matters addressed in the notice of proposed rulemaking (NPRM) published in the February 9, 2012 edition of the Federal Register, 77 FR 6916, on accessibility standards for medical diagnostic equipment and issues raised in the public comments on the NPRM. The Access Board requests applications from interested organizations for representatives to serve on the advisory committee. SUMMARY: E:\FR\FM\13MRP1.SGM 13MRP1 Federal Register / Vol. 77, No. 49 / Tuesday, March 13, 2012 / Proposed Rules DATES: Submit applications by April 27, 2012. Submit applications by any of the following methods: • Mail or Hand Delivery/Courier: Office of Technical and Information Services, Architectural and Transportation Barriers Compliance Board, 1331 F Street NW., suite 1000, Washington, DC 20004–1111. • Fax: 202–272–0081. • Email: pace@access-board.gov. FOR FURTHER INFORMATION CONTACT: Rex Pace, Office of Technical and Information Services, Architectural and Transportation Barriers Compliance Board, 1331 F Street NW., suite 1000, Washington, DC 20004–1111. Telephone: (202) 272–0023 (Voice) or (202) 272–0052 (TTY). Email address: pace@access-board.gov. SUPPLEMENTARY INFORMATION: Section 510 of the Rehabilitation Act (29 U.S.C. 794f) requires the Access Board to issue accessibility standards for medical diagnostic equipment, in consultation with the Commissioner of the Food and Drug Administration. The Access Board published an NPRM in the February 9, 2012 edition of the Federal Register, 77 FR 6916, proposing the accessibility standards. The proposed standards contain minimum technical criteria to ensure that medical diagnostic equipment, including examination tables, examination chairs, weight scales, mammography equipment, and other imaging equipment used by health care providers for diagnostic purposes are accessible to and usable by individuals with disabilities. The proposed standards are intended to ensure, to the maximum extent possible, independent entry to, use of, and exit from such equipment by individuals with disabilities. The proposed standards do not impose any mandatory requirements on health care providers or medical device manufacturers. However, other agencies may issue regulations or adopt policies that require health care providers subject to the agency’s jurisdiction to acquire accessible medical diagnostic equipment that conforms to the standards. The NPRM and information related to the proposed standards are available on the Access Board’s Web site at: https://www.access-board.gov/ medical-equipment.htm. At its January 11, 2012 meeting, the Access Board voted to form an advisory committee (Committee) to advise the Board on matters addressed in the NPRM. The Committee will make recommendations to the Access Board on the technical criteria proposed in the NPRM and issues raised in public emcdonald on DSK29S0YB1PROD with PROPOSALS ADDRESSES: VerDate Mar<15>2010 14:04 Mar 12, 2012 Jkt 226001 comments on the NPRM, including responses to the questions in the NPRM. The comment period on the NPRM ends on June 8, 2012. The Access Board will conduct a preliminary analysis of the public comments and plans to schedule the first meeting of the Committee in September 2012. The Committee is expected to hold four meetings and present a report with its recommendations to the Access Board within two months of the Committee’s first meeting. The Access Board requests applications for representatives of the following interests for membership on the Committee: • Medical device manufacturers; • Health care providers; • Standards setting organizations; • Organizations representing individuals with disabilities; • Federal agencies; and • Other organizations affected by the proposed standards. The number of Committee members will be limited so that the Committee’s work can be accomplished effectively. The Committee will be balanced in terms of interests represented. The Access Board encourages organizations with similar interests to submit a single application to represent their interests. Although the Committee will be limited in size, there will be opportunities for the public to present information to the Committee and to comment at each Committee meeting. Federally registered lobbyists may not be appointed to the Committee, pursuant to Presidential Memorandum dated June 18, 2010, entitled ‘‘Lobbyists on Agency Boards and Commissions’’ (https:// www.whitehouse.gov/the-press-office/ presidential-memorandum-lobbyistsagency-boards-and-commissions). Applications should be sent to the Access Board at the address listed at the beginning of this notice. There is no specific application form. The application should include the following information: • Name of the organization; • Interests represented by the organization; • Person who will represent the organization and an alternate, and the title, address, telephone number, and email address for the representative and alternate; • Description of the representative’s qualifications, including engineering, technical, and design expertise; knowledge of making medical diagnostic equipment accessible to individuals with disabilities; or other expertise related to the rulemaking; and PO 00000 Frm 00008 Fmt 4702 Sfmt 4702 14707 • Certification that the representative and alternate are not federally registered lobbyists. Committee members will not be compensated for their service. The Access Board may, at its discretion, pay travel expenses for a limited number of persons who would otherwise be unable to participate on the Committee. Committee members will serve as representatives of their organizations, not as individuals. Committee members will not be considered special government employees and will not be required to file confidential financial disclosure reports. After the applications have been reviewed, the Access Board will publish a notice in the Federal Register announcing the appointment of Committee members and the first meeting of the Committee. The Committee will operate in accordance with the Federal Advisory Committee Act, 5 U.S.C. app 2. All Committee meetings will be held at the Access Board’s office in Washington, DC. Each meeting will be open to the public. A notice of each meeting will be published in the Federal Register at least 15 days in advance of the meeting. Records will be kept of each meeting and made available for public inspection. David Capozzi, Executive Director. [FR Doc. 2012–5964 Filed 3–12–12; 8:45 am] BILLING CODE 8150–01–P DEPARTMENT OF DEFENSE DEPARTMENT OF VETERANS AFFAIRS 38 CFR Part 17 RIN 2900–AN92 Vet Center Services Department of Defense and Department of Veterans Affairs. ACTION: Proposed rule. AGENCY: The Department of Veterans Affairs (VA) proposes to establish in regulation the readjustment counseling currently provided in VA’s Vet Centers to certain veterans of the Armed Forces and members of their immediate families, and to implement provisions of the Caregivers and Veterans Omnibus Health Services Act of 2010 (the 2010 Act) regarding readjustment counseling. Although for several decades VA has provided readjustment counseling to veterans and members of their immediate families, a regulation is now explicitly required by the 2010 Act. The SUMMARY: E:\FR\FM\13MRP1.SGM 13MRP1

Agencies

[Federal Register Volume 77, Number 49 (Tuesday, March 13, 2012)]
[Proposed Rules]
[Pages 14706-14707]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5964]


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ARCHITECTURAL AND TRANSPORTATION BARRIERS COMPLIANCE BOARD

36 CFR Part 1195

[Docket No. ATBCB-2012-0003]
RIN 3014-AA40


Medical Diagnostic Equipment Accessibility Standards

AGENCY: Architectural and Transportation Barriers Compliance Board.

ACTION: Notice of Intent to establish advisory committee.

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

SUMMARY: The Architectural and Transportation Barriers Compliance Board 
(Access Board) announces its intent to establish an advisory committee 
to advise the Board on matters addressed in the notice of proposed 
rulemaking (NPRM) published in the February 9, 2012 edition of the 
Federal Register, 77 FR 6916, on accessibility standards for medical 
diagnostic equipment and issues raised in the public comments on the 
NPRM. The Access Board requests applications from interested 
organizations for representatives to serve on the advisory committee.

[[Page 14707]]


DATES: Submit applications by April 27, 2012.

ADDRESSES: Submit applications by any of the following methods:
     Mail or Hand Delivery/Courier: Office of Technical and 
Information Services, Architectural and Transportation Barriers 
Compliance Board, 1331 F Street NW., suite 1000, Washington, DC 20004-
1111.
     Fax: 202-272-0081.
     Email: board.gov">pace@access-board.gov.

FOR FURTHER INFORMATION CONTACT: Rex Pace, Office of Technical and 
Information Services, Architectural and Transportation Barriers 
Compliance Board, 1331 F Street NW., suite 1000, Washington, DC 20004-
1111. Telephone: (202) 272-0023 (Voice) or (202) 272-0052 (TTY). Email 
address: board.gov">pace@access-board.gov.

SUPPLEMENTARY INFORMATION: Section 510 of the Rehabilitation Act (29 
U.S.C. 794f) requires the Access Board to issue accessibility standards 
for medical diagnostic equipment, in consultation with the Commissioner 
of the Food and Drug Administration. The Access Board published an NPRM 
in the February 9, 2012 edition of the Federal Register, 77 FR 6916, 
proposing the accessibility standards. The proposed standards contain 
minimum technical criteria to ensure that medical diagnostic equipment, 
including examination tables, examination chairs, weight scales, 
mammography equipment, and other imaging equipment used by health care 
providers for diagnostic purposes are accessible to and usable by 
individuals with disabilities. The proposed standards are intended to 
ensure, to the maximum extent possible, independent entry to, use of, 
and exit from such equipment by individuals with disabilities. The 
proposed standards do not impose any mandatory requirements on health 
care providers or medical device manufacturers. However, other agencies 
may issue regulations or adopt policies that require health care 
providers subject to the agency's jurisdiction to acquire accessible 
medical diagnostic equipment that conforms to the standards. The NPRM 
and information related to the proposed standards are available on the 
Access Board's Web site at: https://www.access-board.gov/medical-equipment.htm.
    At its January 11, 2012 meeting, the Access Board voted to form an 
advisory committee (Committee) to advise the Board on matters addressed 
in the NPRM. The Committee will make recommendations to the Access 
Board on the technical criteria proposed in the NPRM and issues raised 
in public comments on the NPRM, including responses to the questions in 
the NPRM. The comment period on the NPRM ends on June 8, 2012. The 
Access Board will conduct a preliminary analysis of the public comments 
and plans to schedule the first meeting of the Committee in September 
2012. The Committee is expected to hold four meetings and present a 
report with its recommendations to the Access Board within two months 
of the Committee's first meeting.
    The Access Board requests applications for representatives of the 
following interests for membership on the Committee:
     Medical device manufacturers;
     Health care providers;
     Standards setting organizations;
     Organizations representing individuals with disabilities;
     Federal agencies; and
     Other organizations affected by the proposed standards.
    The number of Committee members will be limited so that the 
Committee's work can be accomplished effectively. The Committee will be 
balanced in terms of interests represented. The Access Board encourages 
organizations with similar interests to submit a single application to 
represent their interests. Although the Committee will be limited in 
size, there will be opportunities for the public to present information 
to the Committee and to comment at each Committee meeting. Federally 
registered lobbyists may not be appointed to the Committee, pursuant to 
Presidential Memorandum dated June 18, 2010, entitled ``Lobbyists on 
Agency Boards and Commissions'' (https://www.whitehouse.gov/the-press-office/presidential-memorandum-lobbyists-agency-boards-and-commissions).
    Applications should be sent to the Access Board at the address 
listed at the beginning of this notice. There is no specific 
application form. The application should include the following 
information:
     Name of the organization;
     Interests represented by the organization;
     Person who will represent the organization and an 
alternate, and the title, address, telephone number, and email address 
for the representative and alternate;
     Description of the representative's qualifications, 
including engineering, technical, and design expertise; knowledge of 
making medical diagnostic equipment accessible to individuals with 
disabilities; or other expertise related to the rulemaking; and
     Certification that the representative and alternate are 
not federally registered lobbyists.
    Committee members will not be compensated for their service. The 
Access Board may, at its discretion, pay travel expenses for a limited 
number of persons who would otherwise be unable to participate on the 
Committee. Committee members will serve as representatives of their 
organizations, not as individuals. Committee members will not be 
considered special government employees and will not be required to 
file confidential financial disclosure reports.
    After the applications have been reviewed, the Access Board will 
publish a notice in the Federal Register announcing the appointment of 
Committee members and the first meeting of the Committee. The Committee 
will operate in accordance with the Federal Advisory Committee Act, 5 
U.S.C. app 2. All Committee meetings will be held at the Access Board's 
office in Washington, DC. Each meeting will be open to the public. A 
notice of each meeting will be published in the Federal Register at 
least 15 days in advance of the meeting. Records will be kept of each 
meeting and made available for public inspection.

David Capozzi,
Executive Director.
[FR Doc. 2012-5964 Filed 3-12-12; 8:45 am]
BILLING CODE 8150-01-P
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