Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Annual Reporting for Custom Device Exemption” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
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FOR FURTHER INFORMATION CONTACT:
FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE-14526, Silver Spring, MD 20993-0002, PRAStaff@fda.hhs.gov.
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On May 14, 2014, the Agency submitted a proposed collection of information entitled “Annual Reporting for Custom Device Exemption” 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 0910-0767. The approval expires on July 31, 2017. A copy of the supporting statement for this information collection is available on the Internet at http://www.reginfo.gov/public/do/PRAMain.
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Dated: July 21, 2014.
Assistant Commissioner for Policy.
[FR Doc. 2014-17482 Filed 7-24-14; 8:45 am]
BILLING CODE 4164-01-P