Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062425 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LIFECATH S PICC Catheter, Percutaneous, Intravascular Product Code 2296.211 Product Usage:: ... | 2 | 06/29/2011 | Vygon Corporation |
| LIFECATH S PICC with Microflash Introducer Catheter, Percutaneous, Intravascular Product Code 2296... | 2 | 06/29/2011 | Vygon Corporation |
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