K-number	K012823
Device name	MODIFICATION TO HANDMASTER
Applicant	Ness-Neuromuscular Electrical Stimulation Systems
Product code	GZI
Device class	Class II
Decision date	Nov 14, 2001
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO HANDMASTER

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