FDA Updates are published frequently. Please check this page often.

• FDA Update - December 20, 05 - Endologix Announces Limited Voluntary Recall of Powerlink System Delivery Catheter
  
  
• FDA Update - December 19 2005 - Class 1 Recall: Baxter Healthcare Corp. Meridian® Hemodialyis (HD) Instrument
  
  
• FDA Update - December 9, 2005 - Draft Guidance for Industry and FDA - Nucleic Acid Based In Vitro Diagnostic Devices for Detection of Microbial Pathogens
  
  
• FDA Update - December 6, 2005 - Boston Scientific Announces Worldwide Recall of Stainless Steel Greenfield® Vena Cava Filters Manufactured Before March 10, 2004
  
  
• FDA Update - December 5, 2005 - FDA Approves First Test to Screen for West Nile Virus
  
  
• FDA Update - November 15, 2005 - Draft Guidance - Special Control for Latex Condoms with and without Spermicidal Lubricant
  
  
• FDA Update - November 11, 2005 - Guidance for Industry and Staff - Pilot Program to Evaluate Proposed Globally Harmonized Alternative for Premarket Procedures
  
  
• FDA Update - November 8, 2005 - Classification of Low Energy Ultrasound Wound Cleaner and Issuance of Related Guidance
  
  
• FDA Update - November 8, 2005 - Issuance of Draft Guidance for Tinnitus Marker Devices
  
  
• FDA Update - October 19, 2005 - FDA Issues Device Cost Analysis Report entitled, -FY 2003 and FY 2004 Unit Costs for the Process of Medical Device Review-
  
  
• FDA Update - October 18, 2005 - United States Marshals Seize Violative Infusion Pumps Made by Baxter Healthcare Corporation
  
  
• FDA Update - October 7, 2005 - Plan B-Victim to a Politicized FDA - We Hope Not!
  
  
• FDA Update - Sept 19, 2005 - FDA Guidance on Inspection of Manufacturing Facilities by Accredited Third Parties
  
  
• FDA Update - August 31, 2005 - FDA Offers Tips about Medical Devices and Hurricane Disasters
  
  
• FDA Update - August 12, 2005 - Medical Device User Fee Rates for 2006
  
  
• FDA Update - August 1, 2005 - Delay in publication of Medical Device User Fees for Fiscal Year 2006