K-number	K062532
Device name	ELECTROPULSE - LOW BACK PAIN
Applicant	Pain Relief Technologies
Product code	NUH
Device class	Class II
Decision date	Feb 9, 2007
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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ELECTROPULSE - LOW BACK PAIN

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