Medical Device Recalls
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1 result found
510(K) Number: K984552 |
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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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Cool-tip RF Generator, for use in percutaneous, laparoscopic, intraoperative coagulation and ablatio... | 2 | 05/10/2006 | Covidien LP |
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