K-number	K863830
Device name	CONSEAL(TM) COLOSTOMY CONTINENCE SYSTEM
Applicant	Coloplast A/S
Product code	EZQ
Device class	Class I
Decision date	Oct 16, 1986
Decision	Substantially Equivalent
Regulation	876.5900

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View the full FDA submission: accessdata.fda.gov

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CONSEAL(TM) COLOSTOMY CONTINENCE SYSTEM

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