View Larger Image US FDA SUD Reprocessing Guidance, 2002 “Supplemental Validation Data” Medical Device User Fee and Modernization Act of 2002, Validation Data in Premarket Notification Submissions (510(k)s) for Reprocessed Single-Use Medical Devices By Dan|2019-09-12T18:37:20+00:00June 1st, 2004|Regulatory Resources|0 Comments Share This Story, Choose Your Platform! FacebookTwitterGoogle+PinterestVkEmail Related Posts Center for Disease Control and Prevention (CDC): Gallery Center for Disease Control and Prevention (CDC): September 18th, 2016 | 0 Comments 2008 Government Accountability Office (GAO) Report: Gallery 2008 Government Accountability Office (GAO) Report: January 1st, 2008 | 0 Comments US GAO Report, 2008 Gallery US GAO Report, 2008 January 1st, 2008 | 0 Comments US FDA 2006 Testimony to Committee on Government Reform Gallery US FDA 2006 Testimony to Committee on Government Reform September 26th, 2006 | 0 Comments US FDA SUD Reprocessing Guidance, 2000 “Enforcement Priorities” Gallery US FDA SUD Reprocessing Guidance, 2000 “Enforcement Priorities” August 1st, 2000 | 0 Comments 2000 Government Accountability Office (GAO) Report: Gallery 2000 Government Accountability Office (GAO) Report: June 1st, 2000 | 0 Comments
