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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K970392
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Avanti®+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous pro... 2 07/15/2021 FEI # 1016427
Cordis Corporation
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introduc... 2 03/15/2016 FEI # 1016427
Cordis Corporation
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