K-number	K955670
Device name	DERMATOUCH LATEX GLOVES
Applicant	Concordia Research Lab
Product code	LYY
Device class	Class I
Decision date	Mar 6, 1996
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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DERMATOUCH LATEX GLOVES

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