K-number	K932332
Device name	PATIENT EXAMINATION GLOVE - POWDERED
Applicant	Sj Medical Products (M) Sdn Bhd
Product code	LYY
Device class	Class I
Decision date	Mar 15, 1994
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PATIENT EXAMINATION GLOVE - POWDERED

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