K-number	K130847
Device name	JINTRONIX REHABILITATION SYSTEM (JRS)
Applicant	Jintronix, Inc.
Product code	LXJ
Device class	Class II
Decision date	Feb 28, 2014
Decision	Substantially Equivalent
Regulation	890.5360

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View the full FDA submission: accessdata.fda.gov

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JINTRONIX REHABILITATION SYSTEM (JRS)

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