K-number	K110716
Device name	EVERYWAY LOW BACK PAIN RELIEF SYSTEM
Applicant	Everyway Medical Instruments Co.,Ltd
Product code	NUH
Device class	Class II
Decision date	Oct 18, 2011
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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EVERYWAY LOW BACK PAIN RELIEF SYSTEM

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