K-number	K915444
Device name	DUPEL IONTOPHORESIS DEVICE
Applicant	Empi
Product code	EGJ
Device class	Class II
Decision date	Jul 15, 1994
Decision	Substantially Equivalent
Regulation	890.5525

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View the full FDA submission: accessdata.fda.gov

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DUPEL IONTOPHORESIS DEVICE

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