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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K992347
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Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB 1 09/15/2021 Cordis Corporation
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B 1 09/15/2021 Cordis Corporation
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB 1 09/15/2021 Cordis Corporation
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C 1 09/15/2021 Cordis Corporation
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A 1 09/15/2021 Cordis Corporation
SUPER TORQUE MB Angiographic Catheter product is labeled in part: "***5F (1.65 mm)***110 cm .038" (... 2 11/17/2011 Cordis Corporation
SUPER TORQUE MB Angiographic Catheter product is labeled in part: "***5F (1.65 mm)***110 cm .038" (... 2 11/17/2011 Cordis Corporation
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