Medical Device Recalls
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1 result found
510(K) Number: K150419 |
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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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miraDry System consisting of the MD4000-MC Console, the MD4000-HP miraDry Handpiece, and the MD4000-... | 2 | 11/06/2015 | Miramar Labs, Inc. |
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