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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 48 Results
510(K) Number: K152605
 
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Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (SGL), REF H74908526511; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (SGL), REF H74908526501; cardiac cathe... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF H74908526502; cardiac cathe... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO TIG4 (5PK), REF H749085262502; cardiac cat... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF H749085261902; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; ... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (SGL), REF H749085263011; c... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265022; ... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265002; ... 1 05/10/2024 Boston Scientific Corporation
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