K-number	K080661
Device name	MODELS TENS 7000, EMS 7500 AND TWIN STIM
Applicant	Koalaty Products, Inc.
Product code	IPF
Device class	Class II
Decision date	Mar 24, 2008
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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MODELS TENS 7000, EMS 7500 AND TWIN STIM

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