K-number	K905069
Device name	IODOSORB GEL
Applicant	Perstorp AB C/O Robert Joel Slomoff
Product code	KOZ
Device class	Class I
Decision date	Jan 31, 1991
Decision	Substantially Equivalent
Regulation	878.4018

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View the full FDA submission: accessdata.fda.gov

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IODOSORB GEL

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