K-number	K895365
Device name	MD-2 IONTOPHORESIS UNIT
Applicant	R. A. Fischer Co. Corp.
Product code	EGJ
Device class	Class II
Decision date	Jun 26, 1990
Decision	Substantially Equivalent — Same Device
Regulation	890.5525

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View the full FDA submission: accessdata.fda.gov

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MD-2 IONTOPHORESIS UNIT

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