Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121694 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Imager II 5F Angiographic Catheters, 5 units per package. | 1 | 03/25/2020 | Boston Scientific Corporation |
Boston Scientific Imager II Angiographic Catheter, a pathway for delivering contrast media to select... | 2 | 06/27/2017 | Boston Scientific Corporation |
Boston Scientific Imager II Angiographic Catheter, M001316581 (5-pack outer package UPN), M00131658... | 2 | 03/23/2017 | Boston Scientific Corporation |
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