Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K970466 |
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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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THUNDER® Steerable Guidewire; Model: LVTNDR190S Medtronic guide wires are steerable guide wires ... | 1 | 11/15/2013 | Medtronic Vascular |
THUNDER® Extra Support Guidewire; Models: THNDR190J, THNDR190S, THNDR300J, THNDR300S Medtronic g... | 1 | 11/15/2013 | Medtronic Vascular |
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