Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K012854 |
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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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Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic d... | 2 | 05/04/2017 | Terumo Medical Corporation |
Pinnacle Destination Guiding Sheath, 6 French, 45 cm, Hockey Stick Tip, Tuohy-Borst Valve, Lot ME07,... | 2 | 06/06/2011 | Terumo Medical Corporation |
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