
[Federal Register Volume 81, Number 176 (Monday, September 12, 2016)]
[Notices]
[Page 62743]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-21877]



[[Page 62743]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2016-N-0628; FDA-2012-N-0306; FDA-2002-N-0323; FDA-
2012-N-0427; FDA-2012-N-0536; FDA-2012-N-0560; FDA-2015-N-3662; FDA-
2012-N-0976; FDA-2013-N-0297; FDA-2012-N-1203; FDA-2011-D-0893; FDA-
2014-N-0189; FDA-2012-N-1210]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approvals

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is publishing a list of 
information collections that have 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, Three White Flint North, 11601 Landsdown 
St., North Bethesda, MD 20852, PRAStaff@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: The following is a list of FDA information 
collections recently approved by OMB under section 3507 of the 
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control 
number and expiration date of OMB approval for each information 
collection are shown in table 1. Copies of the supporting statements 
for the information collections are available on the Internet at http://www.reginfo.gov/public/do/PRAMain. 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.

        Table 1--List of Information Collections Approved by OMB
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                                            OMB control    Date approval
           Title of collection                  No.           expires
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Reporting Associated with New Animal           0910-0032       8/31/2019
 Drug Applications......................
Administrative Detention and Banned            0910-0114       8/31/2019
 Medical Devices........................
Registration of Food Facilities.........       0910-0502       8/31/2019
Inspection by Accredited Persons Program       0910-0510       8/31/2019
 Under the Medical Device User Fee and
 Modernization Act of 2002..............
Medical Device User Fee Cover Sheet--FDA       0910-0511       8/31/2019
 Form 3601..............................
Guidance on Informed Consent for in            0910-0582       8/31/2019
 Vitro Diagnostic Studies Using Leftover
 Human Specimens That Are Not
 Individually Identifiable..............
Guidance for Reagents for Detection of         0910-0584       8/31/2019
 Specific Novel Influenza A Viruses.....
Guidance: Emergency Use Authorization of       0910-0595       8/31/2019
 Medical Products.......................
Prevention of Salmonella Enteritidis in        0910-0660       8/31/2019
 Shell Eggs During Production--
 Recordkeeping and Registration
 Provisions.............................
Information to Accompany Humanitarian          0910-0661       8/31/2019
 Device Exemption Applications and
 Annual Distribution Number Reporting
 Requirements...........................
Guidance for Center for Devices and            0910-0738       8/31/2019
 Radiological Health Appeals Processes..
Deeming Tobacco Products To Be Subject         0910-0768       8/31/2019
 to the FD&C Act........................
Food Labeling: Revision of the Nutrition       0910-0813       7/31/2019
 Facts Label and Supplement Facts Label.
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    Dated: September 6, 2016.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2016-21877 Filed 9-9-16; 8:45 am]
 BILLING CODE 4164-01-P


