Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030476 |
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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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Concentric brand Concentric Retriever® X6 Percutaneous Catheter Model REF 90037 | 2 | 07/20/2004 | Concentric Medical Inc |
Concentric brand Concentric Retriever® X5 Percutaneous Catheter Model REF 90035 | 2 | 07/20/2004 | Concentric Medical Inc |
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