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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: K133607
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InterValve V8 Balloon Aortic Valvuloplasty Catheter, model 172212C110, 192412C110, 212612C110, 2328... 2 05/15/2014 FEI # 3010133561
InterValve Inc
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