Medical Device Recalls
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1 result found
510(K) Number: K162127 |
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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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| Bencox Mirabo PE Liner 36/44 Model Number: H1.L61.3644, UDI: 8806373852343 | 2 | 03/13/2017 | CORENTEC CO., LTD |
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