Medical Device Recalls
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1 result found
510(K) Number: K063210 |
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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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ATTAIN HYBRID® Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain Hybrid guide wire i... | 1 | 11/15/2013 | Medtronic Vascular |
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