K-number	K761340
Device name	OSTOMY KARAYA GUM POWDER
Applicant	Howmedica Corp.
Product code	EZR
Device class	Class I
Decision date	Mar 7, 1977
Decision	Substantially Equivalent
Regulation	876.5900

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View the full FDA submission: accessdata.fda.gov

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OSTOMY KARAYA GUM POWDER

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