K-number	K892077
Device name	PATIENT EXAMINATION GLOVE (LATEX)
Applicant	Forchic Corp. of USA
Product code	LYY
Device class	Class I
Decision date	Sep 21, 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 GLOVE (LATEX)

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