K-number	K161875
Device name	LaserCap300, LaserCap224, LaserCap120, LaserCap80
Applicant	Transdermal Cap, Inc.
Product code	OAP
Device class	Class II
Decision date	Sep 30, 2016
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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LaserCap300, LaserCap224, LaserCap120, LaserCap80

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