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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K161866
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BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ Two Nitinol Guidewire PG, Catalog Number ... 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
BioFlo Midline 5F DL-20cm MST-45 Kit w/ Two Nitinol Guidewires PG, Catalog Number 46-810 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
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