K-number	K080606
Device name	ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE
Applicant	Alatech Healthcare, LLC
Product code	LYY
Device class	Class I
Decision date	Aug 7, 2008
Decision	Substantially Equivalent
Regulation	880.6250

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Source

View the full FDA submission: accessdata.fda.gov

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ALATECH POWDERED LATEX PATIENT EXAMINATION GLOVE

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