K-number	K801629
Device name	COVER-ALL MALE INCONTINENCE DEVICE
Applicant	The Urology Group
Product code	KNX
Device class	Class II
Decision date	Aug 12, 1980
Decision	Substantially Equivalent
Regulation	876.5250

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View the full FDA submission: accessdata.fda.gov

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COVER-ALL MALE INCONTINENCE DEVICE

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