0910-AC30 200304 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Medical Devices; Anesthesiology Devices; Proposed Reclassification of Pressure Regulators for Use With Medical Oxygen Substantive, Nonsignificant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 868.2700 21 CFR 868.5905 21 USC 351 21 USC 360c(e)(1) 21 USC 371 No NPRM 12/00/2003 Undetermined Undetermined 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