Medical Device Recalls
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1 result found
510(K) Number: K160721 |
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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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| Vado Steerable Sheath 8.8F, REF SS8FMU67, packaged in a lidded tray that is within a pouch which is ... | 2 | 02/09/2018 |
FEI # 3009749192 Kalila Medical |
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