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Other FDA Documents - October 2008 Releases
Class I Medical Device Recall: VIBE Technologies, Vibrational Integrated Bio-photonic Energizer (VIBE) Machine Multi-Frequency Field Generator
 October 31, 2008
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, November 14, 2008
October 30, 2008
FDA Public Health Notification: Serious Complications Associated with Transvaginal Placement of Surgical Mesh in Repair of Pelvic Organ Prolapse and Stress Urinary Incontinence
 October 21, 2008
Information on Surgical Mesh for Hernia Repairs
 October 21, 2008
Information on Surgical Mesh for Pelvic Organ Prolapse and Stress Urinary Incontinence
 October 21, 2008
PMA Final Decisions for September 2008
 October 20, 2008
Summary Information for: TAXUS Express2 Paclitaxel-Eluting Coronary Stent System (Monorail, MR and Over-the-Wire, OTW) - In-Stent Restenosis (ISR) Indication
 October 15, 2008
Information on Cell Phones (Updated)
 October 14, 2008
Summary Information for: Hoya iSpheric Model YA-60BB Intraocular Lens
 October 7, 2008
Summary Information for: XIENCE V Everolimus Eluting Coronary Stent System and PROMUS Everolimus Eluting Coronary Stent System
 October 7, 2008
CDRH Learn
 October 6, 2008
Class I Medical Device Recall: Nebion, LLC HLX-8 Magnetic Resonance Device
 October 3, 2008
Consumer Information on: Akreos Posterior Chamber Intraocular Lens - P060022
 October 2, 2008
Consumer Information on: COBAS TaqMan HBV Test For Use With The High Pure System - P050028
 October 2, 2008
Consumer Information on: Hoya iSpheric Model YA-60BB Intraocular Lens - P080004
 October 2, 2008
Class I Medical Device Recall: Medtronic INDURA 1P Intrathecal Catheter, Intrathecal Catheter, Sutureless Pump Connector Revision Kit, and Intrathecal Catheter Pump Segment Revision Kit
 October 1, 2008
Ophthalmic Devices Panel Advisory Meeting, June 10, 2008 - Written Comments
 October 1, 2008
Registration and Listing (Device Establishment Registration and Listing for FY2009 Now Available)
 October 1, 2008
 
 

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