K-number	K052813
Device name	FD TENS 2030, MODEL DFJ24T
Applicant	Fuji Dynamics Limited
Product code	GZJ
Device class	Class II
Decision date	Jan 25, 2006
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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FD TENS 2030, MODEL DFJ24T

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