Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060016 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ThromCat Thrombectomy Catheter System. 7F 2.5 -7.0 mm 150 cm. Catalogue number 63000-01. It is a si... | 2 | 03/08/2007 |
FEI # 1000307073 Kensey Nash Corp |
| ThromCat Thrombectomy Catheter System. Catalog number 63000-01 | 2 | 07/23/2007 |
FEI # 1000307073 Kensey Nash Corp |
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