Medical Device Recalls
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1 result found
510(K) Number: K030108 |
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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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Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofre... | 2 | 03/26/2015 | ArthroCare Medical Corporation |
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