K-number	K891833
Device name	GLOUCH(TM) PATIENT EXAMINATION GLOVES
Applicant	Vadax, Inc.
Product code	LZA
Device class	Class I
Decision date	Aug 22, 1989
Decision	Substantially Equivalent
Regulation	880.6250

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Source

View the full FDA submission: accessdata.fda.gov

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GLOUCH(TM) PATIENT EXAMINATION GLOVES

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