K-number	K960942
Device name	LATEX PATIENT EXAMINATION GLOVE
Applicant	Siam Sempermed Corp., Ltd.
Product code	LYY
Device class	Class I
Decision date	Sep 17, 1996
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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LATEX PATIENT EXAMINATION GLOVE

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