Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K964119 |
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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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| Wallstent Endoscopic Biliary Endoprosthesis- 8mm x 40mm, UPN H965430100 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Wallstent Endoscopic Biliary Endoprosthesis 8mm x 60mm, UPN H965430200 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Wallstent Endoscopic Biliary Endoprosthesis 10mm x 80mm, UPN H965430600 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Wallstent Endoscopic Biliary Endoprosthesis 10mm x 40mm, UPN H965430400 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Wallstent Endoscopic Biliary Endoprosthesis 10mm x 60mm, UPN H965430500 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
| Wallstent Endoscopic Biliary Endoprosthesis 8mm x 80mm, UPN H965430300 | 2 | 03/13/2007 |
FEI # 3001451463 Boston Scientific Corporation |
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