K-number	K934335
Device name	PHORESOR II AUTO, MODEL PM800 MODIFICATION
Applicant	Iomed, Inc.
Product code	EGJ
Device class	Class II
Decision date	Jul 26, 1994
Decision	Substantially Equivalent
Regulation	890.5525

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View the full FDA submission: accessdata.fda.gov

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PHORESOR II AUTO, MODEL PM800 MODIFICATION

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