K-number	K781422
Device name	KWIK-FLO URINAL SYSTEM
Applicant	The Grace Mfg. Co.
Product code	KNX
Device class	Class II
Decision date	Sep 7, 1978
Decision	Substantially Equivalent
Regulation	876.5250

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View the full FDA submission: accessdata.fda.gov

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KWIK-FLO URINAL SYSTEM

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