Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K813462 |
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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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| Manual Biopsy Devices containing AIM system: Chiba Needle, 8 inch/20 cm, 22 gauge, Cat. #40-103, Ma... | 3 | 09/14/2004 |
FEI # 3001451463 Boston Scientific Corporation |
| Manual Biopsy Devices containing AIM system: Chiba Needle, 6 inch/15 cm, 22 gauge, Catalog #40-102,... | 3 | 09/14/2004 |
FEI # 3001451463 Boston Scientific Corporation |
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