0910-AC32 200204 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 First Time Published in The Unified Agenda Proposed 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 12/00/2002 No Undetermined Undetermined NA Not Collected Joseph Sheehan M. 0910 Food and Drug Administration FDA 301 827-2974 301 594-4765 joseph.sheehan@fda.hhs.gov HFZ-215, Center for Devices and Radiological Health, HFZ-215, 1350 Piccard Drive, Rockville MD 20850