0910-AC30 200610 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 Medical Devices; Anesthesiology Devices; Proposed Reclassification of Pressure Regulators for Use With Medical Oxygen and Separate Classification of Oxygen Conserving Devices Routine and Frequent Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 868.2700 21 CFR 868.2750 21 USC 351 21 USC 352 21 USC 360c 21 USC 360i 21 USC 371 No NPRM 12/00/2006 Undetermined Undetermined 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