This PDF is the current document as it appeared on Public Inspection on 09/16/2014 at 08:45 am.
Food and Drug Administration, HHS.
The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Medical Devices; Exception From General Requirements for Informed Consent” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (PRA).Start Further Info
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.End Further Info End Preamble Start Supplemental Information
On July 23, 2014, the Agency submitted a proposed collection of information entitled “Medical Devices; Exception From General Requirements for Informed Consent” 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 Start Printed Page 55801displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910-0586. The approval expires on August 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.Start Signature
Dated: September 11, 2014.
Assistant Commissioner for Policy.
[FR Doc. 2014-22089 Filed 9-16-14; 8:45 am]
BILLING CODE 4164-01-P