Medical Device Recalls
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1 result found
510(K) Number: K132581 |
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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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| MicroCutter Xchange 30 Blue Cartridge, FG-025320; The MicroCutter XCHANGE 30 Blue Cartridge and Mic... | 2 | 12/24/2015 | Cardica, Inc. |
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