K-number	K931827
Device name	CLEANLET, CLEANLET XL & KIDS
Applicant	Gainor Medical Europe, Ltd.
Product code	FMK
Device class	Class II
Decision date	Sep 13, 1993
Decision	Substantially Equivalent
Regulation	878.4850

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View the full FDA submission: accessdata.fda.gov

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CLEANLET, CLEANLET XL & KIDS

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