Medical Device Recalls
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1 result found
510(K) Number: K012812 |
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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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Pinnacle Destination Guiding Sheath, 6 French, 90 cm, Straight Tip, Tuohy-Borst Valve, Lot MD24, MD... | 2 | 06/06/2011 | Terumo Medical Corporation |
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