Letters, Testimony & Filings Comments regarding the Institute of Medicine’s Report, Medical Devices and the Public’s Health: The FDA 510(k) Clearance Process
Letters, Testimony & Filings Petition to Ban Surgical Mesh for Transvaginal Repair of Pelvic Organ Prolapse August 25, 2011
Letters, Testimony & Filings Petition to Ban Bedside Assistant Bed Handles, Model Numbers BA10W and BA10W-6, Manufactured by Bed Handles, Inc. May 4, 2011
Letters, Testimony & Filings Petition to FDA to Ban Powdered and Latex Surgeon’s and Patient Examination Gloves April 26, 2011
Letters, Testimony & Filings Letter on CMS National Coverage Decision for Erythropoiesis Stimulating Agents (ESAs) April 15, 2011
Letters, Testimony & Filings Letter Regarding Appropriate Classification of Electroconvulsive Therapy (ECT) Devices February 24, 2011
Letters, Testimony & Filings Testimony on Classification of Automatic External Defibrillators January 25, 2011
Commentary FDA admits it messed up, revokes approval for ReGen medical device that Public Citizen testified against October 15, 2010