K-number	K910711
Device name	AMPRO SURGEON'S GLOVES
Applicant	American Pro Latex, Inc.
Product code	KGO
Device class	Class I
Decision date	Mar 29, 1991
Decision	Substantially Equivalent
Regulation	878.4460

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View the full FDA submission: accessdata.fda.gov

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AMPRO SURGEON'S GLOVES

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