K-number	K800380
Device name	FES ORTHOSIS MODEL NO. 2000
Applicant	Empi
Product code	GZI
Device class	Class II
Decision date	Mar 17, 1980
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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FES ORTHOSIS MODEL NO. 2000

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