0910-AC30 200904 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; 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 Final Rule Stage No No 21 CFR 868.2700 21 CFR 868.2750 21 CFR 868.5905 21 CFR 868.5910 21 USC 351 21 USC 360 21 USC 360c 21 USC 360e 21 USC 360j 21 USC 371 No NPRM 02/27/2007 72 FR 8643 NPRM Comment Period End 05/29/2007 Final Action 10/00/2009 Undetermined Undetermined Undetermined Undetermined No No 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