Medical Device Recalls
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1 result found
510(K) Number: K070213 |
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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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Medtronic Performer CPB-Universal R2100375. Catologue Number R5100052. The Performer CPB System ... | 2 | 07/23/2007 | Medtronic Perfusion Systems |
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