Medical Device Recalls
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1 result found
510(K) Number: K122389 |
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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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Cutera brand truSculpt infrared System (optional), Massager, Vacuum, radio frequency induced heat, P... | 2 | 12/09/2013 | Cutera, Inc. |
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