K-number	K113686
Device name	KIMONO MICROTHIN WITH AQUA LUBE, REALITY ULTRA LUBRICATED
Applicant	Mayer Laboratories, Inc.
Product code	HIS
Device class	Class II
Decision date	Mar 6, 2012
Decision	Substantially Equivalent
Regulation	884.5300

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View the full FDA submission: accessdata.fda.gov

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KIMONO MICROTHIN WITH AQUA LUBE, REALITY ULTRA LUBRICATED

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