Medical Device Recalls
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1 result found
510(K) Number: K070548 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AesDex, LLC Cardica C-Port Flex-A PLUS Distal Anastomosis System, Catalog Number: FG-000150 The... | 2 | 07/13/2018 | AESDEX |
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