K-number	K891951
Device name	THREE GUN PATIENT EXAMINATION GLOVES
Applicant	Bilwin Corp.
Product code	LYY
Device class	Class I
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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THREE GUN PATIENT EXAMINATION GLOVES

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