K-number	K102637
Device name	DYNAREX ULTRASOUND GEL
Applicant	Dynarex Corporation
Product code	MUI
Device class	Class II
Decision date	Feb 16, 2011
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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DYNAREX ULTRASOUND GEL

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