Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K925015 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Catalog Number: 900010 SUTURE REMOVAL KIT Used by medical staff to perform surgical procedures and... | 2 | 04/14/2016 |
FEI # 2648727 Customed, Inc |
| SUTURE REMOVAL KIT CUSTOMED 100/CS Used by medical staff to perform patient care procedures such a... | 2 | 09/03/2015 |
FEI # 2648727 Customed, Inc |
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