K-number	K960467
Device name	POWDER FREE LATEX EXAMINATION GLOVE
Applicant	Biopro, Inc.
Product code	LYY
Device class	Class I
Decision date	May 24, 1996
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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POWDER FREE LATEX EXAMINATION GLOVE

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