K-number	K954293
Device name	PATIENT EXAMINATION GLOVE (POWDERED)
Applicant	Medline Products Co. , Ltd.
Product code	LYY
Device class	Class I
Decision date	Jul 26, 1996
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 (POWDERED)

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