K-number	K142506
Device name	TensCare KegelFit
Applicant	Tenscare, Ltd.
Product code	KPI
Device class	Class II
Decision date	Apr 20, 2015
Decision	Substantially Equivalent
Regulation	876.5320

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Source

View the full FDA submission: accessdata.fda.gov

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TensCare KegelFit

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