K-number	K162994
Device name	Capillus302, Capillus312, Capillus352
Applicant	Capillus, LLC
Product code	OAP
Device class	Class II
Decision date	Nov 18, 2016
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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Capillus302, Capillus312, Capillus352

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