Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080292 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Epicor LP Connecting Cable, CC-6-LP-CE, Catalog Number 12263, an accessory to the Epicor Cardiac Abl... | 2 | 01/30/2009 | St. Jude Medical Inc |
| St. Jude Medical Epicor UltraWand LP Handheld Ablation Device, model UW-LP-2, Sterilized with Ethyl... | 2 | 06/07/2010 | St. Jude Medical Atrial Fibrillation Division Inc |
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