Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K103014 |
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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. |
MiraDry System consisting of the DTS3000 Console, MiraDry Handpiece (MD3001-HP), the miraDry biotip... | 2 | 06/17/2011 | Miramar Labs, Inc. |
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