K-number	K901855
Device name	LATEX PATIENT EXAMINATION GLOVE
Applicant	Tower Marketing Sdn. Bhd.
Product code	LYY
Device class	Class I
Decision date	May 18, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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Source

View the full FDA submission: accessdata.fda.gov

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LATEX PATIENT EXAMINATION GLOVE

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