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Other FDA Documents - December 2005 Releases
| FDA Centennial and CDRH Milestones |
December 30, 2005 |
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| Second Update of FDA Preliminary Public Health Notification: Guidant VENTAK PRIZM® 2 DR and CONTAK RENEWAL® Implantable Cardioverter Defibrillators |
December 28, 2005 |
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| Summary Information for: ADVIA Centaur® HBc Total ReadyPack Reagents and ADVIA Centaur® HBc Total Quality Control Materials - P040004 |
December 27, 2005 |
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| Summary Information for: VISTAKON® (senofilcon A) Contact Lens, Clear and Visibility Tinted with UV Blocker - P040045 |
December 27, 2005 |
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| PMA Final Decisions for November 2005 |
December 23, 2005 |
| FDA to Scrutinize MQSA Facilities with History of Noncompliance |
December 22, 2005 |
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| To All Electronic Product Manufacturers and Importers: New Product Codes for Radiation-Emitting Electronic Products Now Available |
December 22, 2005 |
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| Endologix Announces Limited Voluntary Recall of Powerlink System Delivery Catheter |
December 21, 2005 |
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| FDA Preliminary Public Health Notfication - Update of Information about Ralstonia spp. Associated with Vapotherm Respiratory Gas Administration Device |
December 21, 2005 |
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| Consumer Information on: C2a – Taper™ Acetabular System |
December 19, 2005 |
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| Class I Recall - Baxter Meridian® Hemodialyis (HD) Instrument |
December 19, 2005 |
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| Summary Information for Epic(TM) and Atlas(R)+ HF CRT-D Systems - P030054/S010 |
December 19, 2005 |
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| FDA Notifies Health Care Professionals of Problem with Baxter Healthcare's Meridian Hemodialysis Instrument - Kinks in Device Tubing Can Pose Serious Risk to Patients |
December 19, 2005 |
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| Learn About Medical Device Recalls |
December 16, 2005 |
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| FDA Class I Classification Given to Baxter’s September 2005 Urgent Product Recall for Meridian Hemodialysis Instrument |
December 14, 2005 |
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| Personal Protective Equipment (PPE) and Patient Care |
December 13, 2005 |
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| Consumer Information on: IBI Therapy ™ Dual 8 ™ Ablation Catheter and IBI 1500T6 ( USA ) Generator |
December 7, 2005 |
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| Ultraviolet Radiation Burns from High Intensity Metal Halide and Mercury Vapor Lighting Remain a Public Health Concern |
December 7, 2005 |
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| Boston Scientific Announces Worldwide Recall of Stainless Steel Greenfield (R) Vena Cava Filters Manufactured Before March 10, 2004 |
December 6, 2005 |
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| Convenience Kits Interim Regulatory Guidance |
December 6, 2005 |
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| Consumer Information on: IBI Therapy (TM) Dual 8 (TM) Ablation Catheter and IBI 1500T6 ( USA ) Generator |
December 5, 2005 |
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| 510(k)s Final Decisions Rendered for November 2005 |
December 5, 2005 |
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| FDA Approves First Test to Screen for West Nile Virus in Donors of Blood, Organs, Cells and Tissues |
December 2, 2005 |
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