Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K892530 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 | 2 | 12/19/2019 | Arrow International Inc |
| Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J | 2 | 12/19/2019 | Arrow International Inc |
| Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon ... | 2 | 04/04/2013 | Arrow International Inc |
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