Medical Device Recalls
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1 result found
510(K) Number: K162214 |
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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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TandemLife ECLS Procedure Kit - V24/A17, Catalog Number 5740-2417 - Product Usage: The function of ... | 2 | 02/07/2020 | Cardiac Assist, Inc |
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