Medical Device Recalls
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1 result found
510(K) Number: K021249 |
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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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FlexShaft, product code FS14; FlexShaft II, product code FS214; FlexShaft III, product code FS312; F... | 2 | 11/23/2009 | Surgical Devices/Covidien |
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