K-number	K053468
Device name	NESS L300
Applicant	Ness-Neuromuscular Electrical Stimulation Systems
Product code	GZI
Device class	Class II
Decision date	Jul 7, 2006
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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NESS L300

Everything you need for a 510(k) submission. Nothing you don't.