Medical Device Recalls
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1 result found
510(K) Number: K082349 |
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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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FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm, Maximum Guidewire Diam... | 2 | 03/27/2014 | Medtronic Vascular, Inc. |
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