K-number	K964629
Device name	VINYL PATIENT EXAMINATION GLOVES
Applicant	Arista Medi Prima
Product code	LYZ
Device class	Class I
Decision date	Feb 10, 1997
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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VINYL PATIENT EXAMINATION GLOVES

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