K-number	K894454
Device name	PATIENT EXAMINATION GLOVES, LATEX
Applicant	Windwell Agencies Sdn. Bhd.
Product code	LYY
Device class	Class I
Decision date	Sep 26, 1989
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PATIENT EXAMINATION GLOVES, LATEX

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