K-number	K883556
Device name	LATEX SURGICAL GLOVE (NON STERILE)
Applicant	Makintech Corp.
Product code	KGO
Device class	Class I
Decision date	Feb 3, 1989
Decision	Substantially Equivalent
Regulation	878.4460

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View the full FDA submission: accessdata.fda.gov

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LATEX SURGICAL GLOVE (NON STERILE)

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