Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151260 |
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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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ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethyl... | 2 | 04/10/2017 | Cardiovascular Systems Inc |
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Numb... | 2 | 04/10/2017 | Cardiovascular Systems Inc |
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