K-number	K122061
Device name	K-Y BRAND LIQUIBEADS
Applicant	Johnson & Johnson Healthcare Products
Product code	NUC
Device class	Class II
Decision date	Nov 8, 2013
Decision	Substantially Equivalent
Regulation	884.5300

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Source

View the full FDA submission: accessdata.fda.gov

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K-Y BRAND LIQUIBEADS

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