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Other FDA Documents - Archives
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Other FDA Documents - May Releases
Acanthamoeba Keratitis Infections Potentially Related to Complete MoisturePlus Multipurpose Contact Lens Solution Manufactured by Advanced Medical Optics (AMO)
 May 31, 2007
Advice for Patients With Soft Contact Lenses: Acanthamoeba Keratitis Infections Related to Complete MoisturePlus Multi Purpose Contact Lens Solution
 May 31, 2007
Class I Medical Device Recall: Integra LifeSciences Corporation (also known as Integra NeuroSciences) EnDura No-React Dural Substitute
 May 31, 2007
Medical Devices Dispute Resolution Panel Meeting, December 15, 2006 - Minutes
 May 30, 2007
Advanced Medical Optics Voluntarily Recalls Complete MoisturePlus Contact Lens Solution
 May 29, 2007
MDUFMA Public Stakeholder Meeting Transcript - April 30, 2007
May 29, 2007
Consumer Information on: Mynx Vascular Closure System - P040044S1
 May 25, 2007
Class I Medical Device Recall: Ortho-Clinical Diagnostics, Inc. VITROS Immunodiagnostic Products Troponin I Reagent Pack
 May 24, 2007
Consumer Information on: CORDIS ENTERPRISE Vascular Reconstruction Device and Delivery System - H060001 of Heart Valves and Valve Conduits, Annuloplasty Rings, Surgical Grafts, Meshes and Other Devices Manufactured by Shelhigh, Inc. (Updated 5/18)
 May 22, 2007
Pilot Multi-Purpose Audit Program (PMAP) - Questions and Answers Related to the Pilot
 May 22, 2007
FDA & YOU - News for Health Educators and Students - Spring 2007
 May 21, 2007
FDA Preliminary Public Health Notification: Possible Contamination and Malfunction of Heart Valves and Valve Conduits, Annuloplasty Rings, Surgical Grafts, Meshes and Other Devices Manufactured by Shelhigh, Inc. (Updated 5/18)
 May 18, 2007
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, February 22, 2007 - Minutes
 May 16, 2007
Product Codes for Radiation-Emitting Electronic Products
 May 16, 2007
Consumer Information on: IMMULITE/IMMULITE 1000 and IMMULITE 2000 Free PSA - P060005
 May 15, 2007
PMA Final Decisions for April 2007
 May 15, 2007
Medical Devices Dispute Resolution Panel Advisory Meeting, April 19, 2007 - Transcripts
 May 14, 2007
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, April 24, 2007 - Transcripts
 May 14, 2007
Summary Information for: C-flex Model 570C Intraocular Lens (IOL)
 May 11, 2007
Circulatory System Devices Panel Advisory Meeting, June 27, 2007 - Notice of Meeting
 May 11, 2007
Consumer Information on: EMS Swiss Dolorclast - P050004
 May 11, 2007
Nationwide Evaluation of X-Ray Trends (NEXT) - Tabulation and Graphical Summary of 2000 Survey of Computed Tomography
 May 11, 2007
Summary Information for: Perlane Injectable Gel
 May 11, 2007
Summary Information for: Vascular Solutions D-Star Flowable Hemostat
 May 11, 2007
FDA Clears First Respirators for Use in Public Health Medical Emergencies
May 10, 2007
Consumer Information on: IBI Therapy Cool Path Ablation Catheter and IBI 1500T9 RF Generator - P060019
 May 9, 2007
General Hospital and Personal Use Devices Panel Advisory Meeting, May 4, 2007 - Brief Summary
 May 8, 2007
510(k) Final Decisions - April 2007
 May 7, 2007
Consumer Information on: Onyx Liquid Embolic System (Onyx HD-500) - H060003
 May 7, 2007
Information on Radiofrequency Identification (RFID)
 May 3, 2007
Consumer Information on: ACUITY Steerable Lead Models 4554, 4555, and 4556 - P050046
 May 2, 2007
FDA Requests Recall of All Shelhigh Medical Devices
 May 2, 2007
General Hospital and Personal Use Devices Panel Advisory Meeting, May 4, 2007 - Agenda, Roster, Briefing, Questions
 May 2, 2007
Consumer Information on: MONOLISA Anti-HBc EIA - P060031
 May 2, 2007
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, April 24, 2007 - Questions, Slides
 May 2, 2007
Questions & Answers on Shelhigh Medical Devices (May 2, 2007)
 May 2, 2007