Medical Device Recalls
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1 result found
510(K) Number: K801404 |
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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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Cardiopulmonary bypass connector; P/N: 321334-000 DESC: CONNECTOR, 3/8 X 3/8 X 1/2 CLEAR PAY LOT: 29... | 2 | 11/06/2014 | Dokitz NovoSci |
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