Medical Device Recalls
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1 result found
510(K) Number: K850385 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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DLP(R) Pericardial/Intracardiac Sump Cannulae, 20 Fr., P/N: 12112. This product is intended for dra... | 2 | 01/26/2009 | Medtronic Cardiovascular Revascularization & Surgical Therap |
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