Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Premarket Approval of Medical Devices-21 CFR Part 814, 3210 [2014-00870]

Download as PDF 3210 Federal Register / Vol. 79, No. 12 / Friday, January 17, 2014 / Notices that a collection of information entitled ‘‘Guidance for Industry and Food and Drug Administration Staff on Dear Health Care Provider Letters: Improving Communication of Important Safety Information’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, PRAStaff@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On September 13, 2012, the Agency submitted a proposed collection of information entitled ‘‘Guidance for Industry and Food and Drug Administration Staff on Dear Health Care Provider Letters: Improving Communication of Important Safety Information’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0754. The approval expires on December 31, 2016. A copy of the supporting statement for this information collection is available on the Internet at https:// www.reginfo.gov/public/do/PRAMain. Dated: January 13, 2014. Leslie Kux, Assistant Commissioner for Policy. BILLING CODE 4160–01–P Food and Drug Administration, HHS. emcdonald on DSK67QTVN1PROD with NOTICES Notice. The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Premarket Approval of Medical Devices—21 CFR Part 814’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. 17:00 Jan 16, 2014 Jkt 232001 Dated: January 13, 2014. Leslie Kux, Assistant Commissioner for Policy. [FR Doc. 2014–00869 Filed 1–16–14; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–N–0618] Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Reporting and Recordkeeping for Electronic Products—General Requirements AGENCY: Food and Drug Administration ACTION: [Docket No. FDA–2013–N–0804] SUMMARY: Food and Drug Administration, Notice. The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Premarket Notification Submission 510(k), Subpart E’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, PRAStaff@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On November 12, 2013, the Agency submitted a proposed collection of information entitled ‘‘Premarket Notification Submission 510(k), Subpart E’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is SUMMARY: Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Premarket Approval of Medical Devices—21 CFR Part 814 not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0120. The approval expires on January, 31 2017. A copy of the supporting statement for this information collection is available on the Internet at https://www.reginfo.gov/ public/do/PRAMain. DEPARTMENT OF HEALTH AND HUMAN SERVICES ACTION: [Docket No. FDA–2013–N–0485] VerDate Mar<15>2010 BILLING CODE 4160–01–P HHS. Food and Drug Administration SUMMARY: [FR Doc. 2014–00870 Filed 1–16–14; 8:45 am] AGENCY: DEPARTMENT OF HEALTH AND HUMAN SERVICES ACTION: Dated: January 13, 2014. Leslie Kux, Assistant Commissioner for Policy. Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Premarket Notification Submission 510(k) [FR Doc. 2014–00872 Filed 1–16–14; 8:45 am] AGENCY: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, PRAStaff@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On November 22, 2013, the Agency submitted a proposed collection of information entitled ‘‘Premarket Approval of Medical Devices—21 CFR Part 814’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0231. The approval expires on January 31, 2017. A copy of the supporting statement for this information collection is available on the Internet at https://www.reginfo.gov/ public/do/PRAMain. FOR FURTHER INFORMATION CONTACT: PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 Food and Drug Administration, HHS. Notice. The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Reporting and Recordkeeping for Electronic Products—General Requirements’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, Food and Drug Administration, 1350 Piccard Dr., PI50–400B, Rockville, MD 20850, PRAStaff@fda.hhs.gov. SUPPLEMENTARY INFORMATION: On November 20, 2013, the Agency submitted a proposed collection of information entitled ‘‘Reporting and Recordkeeping for Electronic Products— General Requirements’’ to OMB for review and clearance under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0025. The approval expires on January 31, 2017. A copy of the supporting statement for this information collection is available on E:\FR\FM\17JAN1.SGM 17JAN1

Agencies

[Federal Register Volume 79, Number 12 (Friday, January 17, 2014)]
[Notices]
[Page 3210]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-00870]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2013-N-0485]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approval; Premarket Approval of Medical 
Devices--21 CFR Part 814

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Premarket Approval of Medical 
Devices--21 CFR Part 814'' has been approved by the Office of 
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: FDA PRA Staff, Office of Operations, 
Food and Drug Administration, 1350 Piccard Dr., PI50-400B, Rockville, 
MD 20850, PRAStaff@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: On November 22, 2013, the Agency submitted a 
proposed collection of information entitled ``Premarket Approval of 
Medical Devices--21 CFR Part 814'' to OMB for review and clearance 
under 44 U.S.C. 3507. An Agency may not conduct or sponsor, and a 
person is not required to respond to, a collection of information 
unless it displays a currently valid OMB control number. OMB has now 
approved the information collection and has assigned OMB control number 
0910-0231. The approval expires on January 31, 2017. A copy of the 
supporting statement for this information collection is available on 
the Internet at https://www.reginfo.gov/public/do/PRAMain.

    Dated: January 13, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-00870 Filed 1-16-14; 8:45 am]
BILLING CODE 4160-01-P

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