Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K924607 |
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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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Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-0... | 2 | 03/07/2016 | Arrow International Inc |
Arrow Super Arrow-Flex Percutaneous Sheath Introducers | 2 | 06/24/2009 | Arrow International Inc |
10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set | 3 | 11/01/2003 | Arrow International Inc |
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