Medical Device Recalls
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1 result found
510(K) Number: K131694 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVE... | 2 | 10/05/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
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