0910-AC32 200504 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Medical Devices; Patient Examination and Surgeons' Gloves; Adulteration Substantive, Nonsignificant Previously Published in The Unified Agenda Final Rule Stage No No 21 CFR 800.20 21 USC 321 21 USC 331 21 USC 351 21 USC 352 21 USC 371 21 USC 374 No NPRM 03/31/2003 68 FR 15404 NPRM Comment Period End 06/30/2003 Final Action 12/00/2005 No Undetermined Undetermined NA Not Collected Madhusoodana Nambiar 0910 Food and Drug Administration FDA 301 796-5837 301 847-8145 madhusoodana.nambiar@fda.hhs.gov Center for Devices and Radiological Health, WO 66, Room 5518, 10903 New Hampshire Avenue, Silver Spring MD 20993