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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K103014
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miraDry System consisting of the MD4000-MC Console, the MD4000-HP miraDry Handpiece, and the MD4000-... 2 11/06/2015 FEI # 3008082710
Miramar Labs, Inc.
MiraDry System consisting of the DTS3000 Console, MiraDry Handpiece (MD3001-HP), the miraDry biotip... 2 06/17/2011 FEI # 3008082710
Miramar Labs, Inc.
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