K-number	K925030
Device name	SURGEON'S GLOVE
Applicant	Wuhrlin Soplamed (M) Sdn Bhd
Product code	KGO
Device class	Class I
Decision date	Jul 13, 1993
Decision	Substantially Equivalent
Regulation	878.4460

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Source

View the full FDA submission: accessdata.fda.gov

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SURGEON'S GLOVE

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