K-number	K895642
Device name	LATEX PATIENT EXAMINATION GLOVES
Applicant	Siam Sempermed Corp., Ltd.
Product code	OPE
Device class	Class unclassified
Decision date	Dec 5, 1989
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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LATEX PATIENT EXAMINATION GLOVES

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