K-number	K192012
Device name	Capillus 112, Capillus 244
Applicant	Capillus
Product code	OAP
Device class	Class II
Decision date	Sep 12, 2019
Decision	Substantially Equivalent
Regulation	890.5500

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Source

View the full FDA submission: accessdata.fda.gov

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Capillus 112, Capillus 244

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