Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K050456 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization proce... | 2 | 02/21/2013 | Medrad Inc |
| MEDRAD Avanta Fluid Management Injection System, Catalog numbers: AVA 500 TABL, AVA 500 PEDL Pro... | 2 | 07/22/2011 | Medrad Inc |
| Avanta Fluid Management Injection System, Avanta Multi-Patient Disposable Set (MPAT) High Pressure C... | 2 | 03/23/2010 | Medrad Inc |
| Medrad Avanta Single Patient Disposable Sets. Catalog number AVA 500 SPAT | 2 | 10/21/2005 | Medrad Inc |
| Medrad Avanta Multi-patient Disposable Sets. Catalog number AVA 500 MPAT | 2 | 10/21/2005 | Medrad Inc |
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