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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: K092486
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Vortex MEDICAL AngioVac Circuit, REF/UPN VTX3100, STERILE, Rx Only, Single Use Only -- The AngioVac ... 2 05/20/2016 FEI # 3017892510
Angiodynamics Inc. (Navilyst Medical Inc.)
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