K-number	K121925
Device name	POWDERED LATEX SURGEON'S GLOVE
Applicant	Suzhou Colour-Way Enterprise Development Co., Ltd.
Product code	KGO
Device class	Class I
Decision date	Aug 28, 2013
Decision	Substantially Equivalent
Regulation	878.4460

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View the full FDA submission: accessdata.fda.gov

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POWDERED LATEX SURGEON'S GLOVE

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