Medical Device Recalls
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1 result found
510(K) Number: K955839 |
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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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| Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indi... | 1 | 12/02/2016 | Centurion Medical Products Corporation |
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