Medical Device Recalls
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1 result found
510(K) Number: K091329 |
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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® Peripheral Guiding Sheath, 8 French, 90cm, Straight Tip, Cross Cut Valve. ... | 2 | 06/27/2013 | Terumo Medical Corporation |
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