Medical Device Recalls
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1 result found
510(K) Number: K073001 |
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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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Intelligent Delivery System, Straight, product code iDriveS; Intelligent Delivery System, Curved, pr... | 2 | 11/23/2009 | Surgical Devices/Covidien |
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