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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 AL1 (5PK), REF H74908526962; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL2 (5PK), REF H74908526982; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL3 (5PK), REF H749085261002; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR MOD (5PK), REF H74908526892; cardiac c... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CAS1 (5PK), REF H749085261712; cardiac cat... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS2.5 (5PK), REF H74908526572A2; cardiac... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3 (5PK), REF H74908526573A2; cardiac c... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A2; cardiac... 1 05/10/2024 Boston Scientific Corporation
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