Medical Device Recalls
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1 result found
510(K) Number: K120988 |
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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 DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedure... | 2 | 03/05/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
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