[Federal Register Volume 84, Number 202 (Friday, October 18, 2019)]
[Notices]
[Pages 55972-55973]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-22803]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket Nos. FDA-2013-N-0370, FDA-2013-N-0065, FDA-2012-N-0427, FDA-
2012-N-0536, FDA-2012-N-0873, FDA-2015-N-3662, FDA-2012-N-0976, FDA-
2013-N-0297, FDA-2011-D-0893, and FDA-2019-N-1265]


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: Ila S. Mizrachi, Office of Operations, 
Food and Drug Administration, Three White Flint North, 10A-12M, 11601 
Landsdown St., North Bethesda, MD 20852, 301-796-7726, 
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 
https://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.

[[Page 55973]]



        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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Export of Medical Devices; Foreign             0910-0264       8/31/2022
 Letters of Approval....................
Registration of Food Facilities.........       0910-0502       8/31/2022
Inspection by Accredited Persons Program       0910-0510       8/31/2022
 Under the Medical Device User Fee and
 Modernization Act of 2002..............
Medical Device User Fee Cover Sheet--          0910-0511       8/31/2022
 Form FDA 3601..........................
Bar Code Label Requirement for Human           0910-0537       8/31/2022
 Drug Products and Biological Products..
Guidance on Reagents for Detection of          0910-0584       8/31/2022
 Specific Novel Influenza A Viruses.....
Guidance: Emergency Use Authorization of       0910-0595       8/31/2022
 Medical Products and Related
 Authorities............................
Production, Storage, and Transportation        0910-0660       8/31/2022
 of Shell Eggs (preventing Salmonella
 Enteritidis (SE))......................
Center for Devices and Radiological            0910-0738       8/31/2022
 Health Appeals Processes...............
Food Labeling: Nutrition Facts Label and       0910-0813       8/31/2022
 Supplement Facts Labels................
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    Dated: October 10, 2019.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2019-22803 Filed 10-17-19; 8:45 am]
 BILLING CODE 4164-01-P


