K-number	K072123
Device name	HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE
Applicant	Biowave Corporation
Product code	GZJ
Device class	Class II
Decision date	Feb 1, 2008
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE

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