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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K062414
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Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for ... 2 04/21/2021 FEI # 3017892510
Angiodynamics Inc. (Navilyst Medical Inc.)
8F Smart Port CT, Catalog number: CT80STPD and CT80STPD-NF; AngioDynamics, INC. The Smart Port ... 2 10/13/2011 FEI # 3017892510
Angiodynamics, INC
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