FDA 510(k), K163170, Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352

FDA 510(k), K163170, Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352

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510(K) Number: K163170
Device Name: Capillus 82, Capillus 202, Capillus 272 Pro, 272 Office Pro, Capillus 302, Capillus 312, and Capillus 352
Manufacturer: CAPILLUS, LLC
Device Classification Name: laser, comb, hair
Regulation Number: 890.5500
Classification Product Code: OAP
Date Received: 11/14/2016
Decision Date: 01/31/2017
Regulation Medical Specialty: Physical Medicine

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