K-number	K192733
Device name	RelieforMe TENS/EMS Device Model UPK-GE01
Applicant	Umeheal , Ltd.
Product code	IPF
Device class	Class II
Decision date	Dec 23, 2019
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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RelieforMe TENS/EMS Device Model UPK-GE01

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