0910-AF77 200804 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Natural Rubber-Containing Medical Device; User Labeling Other Significant Previously Published in The Unified Agenda Completed Actions No No Completion of a Section 610 Review 21 CFR 801.437 21 USC 321 21 USC 331 21 USC 351 21 USC 352 21 USC 357 21 USC 360i 21 USC 360j 21 USC 371 21 USC 374 Statutory Other 09/30/2007 Planned section 610 review No Final Action 09/30/1997 62 FR 51021 Begin Review of Current Regulation 01/02/2007 End Review of Current Regulation 12/28/2007 No None No Undetermined Yes 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