Medical Device Recalls
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1 result found
510(K) Number: K160257 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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SHIP KIT, PROCEDURE KIT, PROTEKDUO LS - DL31 for temporary Cardiopulmonary bypass. Including the fol... | 3 | 11/29/2021 | Cardiac Assist, Inc |
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