K-number	K913531
Device name	PATIENT EXAMINATION GLOVEWS
Applicant	Pt. Sarana Indoprotex
Product code	LYY
Device class	Class I
Decision date	Jan 7, 1992
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PATIENT EXAMINATION GLOVEWS

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