Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932925 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Boston Scientific Vesica Drill-In Bone Locator; sterile, single use only; REF/Catalog no. 820-103, U... | 2 | 08/02/2006 |
FEI # 1828132 Boston Scientific Corp |
| Boston Scientific Vesica Sling Kits with Drill-In Anchor System sterile, for single use only; Ref/Ca... | 2 | 08/02/2006 |
FEI # 1828132 Boston Scientific Corp |
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