K-number	K973831
Device name	PRE-POWDERED PATIENT EXAMINATION GLOVE
Applicant	Safe Glove , Ltd.
Product code	LYY
Device class	Class I
Decision date	Jan 6, 1998
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PRE-POWDERED PATIENT EXAMINATION GLOVE

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