Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K050863 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Boston Scientific, Imager II Angiographic Catheter, (Outer Carton Label): UPN M001315081, 5 Fr, 100... | 3 | 12/06/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Imager" II Angiographic Catheters, Sterilized with ethylene oxide gas, Manufactured for Boston Scien... | 2 | 01/21/2010 |
FEI # 3002095335 Boston Scientific Corporation |
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