Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062414 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for ... | 2 | 04/21/2021 | Angiodynamics Inc. (Navilyst Medical Inc.) |
8F Smart Port CT, Catalog number: CT80STPD and CT80STPD-NF; AngioDynamics, INC. The Smart Port ... | 2 | 10/13/2011 | Angiodynamics, INC |
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