K-number	K052289
Device name	DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE
Applicant	Biowave Corporation
Product code	LIH
Device class	Class II
Decision date	Dec 13, 2005
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE

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