K-number	K900933
Device name	PROTEX LATEX EXAMINATION GLOVES
Applicant	Seyen Intl., Inc.
Product code	LYY
Device class	Class I
Decision date	Mar 27, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PROTEX LATEX EXAMINATION GLOVES

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