Medical Device Recalls
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1 result found
510(K) Number: K021899 |
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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 7F Balloon Guide Catheter (percutaneous catheter per 21 CFR 870.1250), REF 90072, manufac... | 2 | 01/12/2011 | Concentric Medical Inc |
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