Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K904694 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ANGIODRAPE PACK DAMAS 6/CS Used by medical staff to perform surgical procedures and patient car... | 2 | 09/03/2015 | Customed, Inc |
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