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Other FDA Documents - Archives
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Other FDA Documents - April Releases
FDA Preliminary Public Health Notification: Important Safety Recommendations for Baxter's Colleague Infusion Pumps
 April 28, 2006
Medical Device Industry Perspectives on MDUFMA: Final Report (Prepared by The Lewin Group, Inc.)
 April 26, 2006
FDA AND NIOSH Public Health Notification: Oxygen Regulator Fires Resulting from Incorrect Use of CGA 870 Seals
 April 25, 2006
PMA Final Decisions Rendered for March 2006
 April 21, 2006
Summary of Safety and Probable Benefit - Karl Storz Semi-Rigid TTTS Fetoscopy Instrument Set - H040005
 April 20, 2006
Summary Information for: Ceralas I Laser System and Ceralink Slit Lamp Adapter - P050021
 April 18, 2006
Class 1 Recall - Ortho-Clinical Diagnostics Immunodiagnostic Products Signal Reagent
April 18, 2006
Summary Information for: Quantel Activis Laser and ZSL30 ACT, and HSBMBQ ACT Slit Lamp Adapters - P050026
April 18, 2006
Blackstone Medical, Inc. Issues Voluntary Recall of ICON(TM) Modular Fixation System
 April 17, 2006
Boca Medical Products, Inc. Issues Nationwide Recall of Insulin Syringe Product
 April 14, 2006
Contact Lenses and Eye Infections
 April 14, 2006
Letter for 2007 Cycle of Annual Registration of Device Establishments
 April 12, 2006
Summary Information for: LUMA™ Cervical Imaging System - P040028
 April 12, 2006
Stakeholder Meeting to Discuss the Possible Implementation of Two Review Performance Goals in the Medical Device User Fee and Modernization Act of 2002; Public Meeting - May 22, 2006
 April 12, 2006
Advice for Patients With Soft Contact Lenses: Risk of Serious Fungal Infection
 April 10, 2006
FDA Preliminary Public Health Notification - Fungal Keratitis Infections Related to Contact Lens Use
 April 10, 2006
Investigation of Serious Eye Infections Associated With Soft Contact Lens Use and Contact Lens Solution
April 10, 2006
Use of Wireless Communication Devices and the Risk of Brain Cancer
April 6, 2006
510(k) Final Decisions - March 2006
 April 5, 2006
Disetronic Medical Systems, Inc. Announces a Voluntary Nationwide Recall Of All ACCU-CHEK Ultraflex Infusion Sets
 April 4, 2006
FDA Approves Humanitarian Device Exemption for Treatment of Fetuses With Twin-To-Twin Transfusion Syndrome
 April 4, 2006
Consumer Information on: Karl Storz Rigid TTTS Fetoscopy Instrument Set
 April 4, 2006