Senior Advisor for Patient Safety

0910-AG31 201110 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Unique Device Identification Economically Significant Previously Published in The Unified Agenda Proposed Rule Stage Yes No 21 CFR 16 21 CFR 801 21 CFR 803 21 CFR 806 21 CFR 810 21 CFR 814 21 CFR 820 21 CFR 821 21 CFR 822 Not Yet Determined Yes NPRM 01/00/2012 Yes Businesses None Undetermined No Yes No John Crowley J. Senior Advisor for Patient Safety 0910 Food and Drug Administration FDA 301 980-1936 jay.crowley@fda.hhs.gov Center for Devices and Radiological Health, WO 66, Room 2315, 10903 New Hampshire Avenue, Silver Spring MD 20993