Medical Device Recalls
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1 result found
510(K) Number: K102725 |
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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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BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescript... | 2 | 07/24/2012 | Bridgepoint Medical |
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