Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K961390 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter, 35mm Vascular/Thin, Pr... | 2 | 12/17/2003 | Ethicon Endo-Surgery |
| Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter, 35mm Standard, Product... | 2 | 12/17/2003 | Ethicon Endo-Surgery |
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