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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K021899
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Concentric 7F Balloon Guide Catheter (percutaneous catheter per 21 CFR 870.1250), REF 90072, manufac... 2 01/12/2011 FEI # 3003271051
Concentric Medical Inc
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