Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K926467 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cobe Optima XP Hollow Fiber Membrane Oxygenator, Sterile, (Custom Heart/Lung Packs), Catalog Numbers... | 2 | 08/24/2006 | Cobe Cardiovascular, Inc |
| Cobe Optima XP Hollow Fiber Membrane Oxygenator/Reservoir, Sterile, (Standalone Systems) Catalog Num... | 2 | 08/24/2006 | Cobe Cardiovascular, Inc |
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