K-number	K902278
Device name	PVC PATIENT EXAMINATION GLOVE
Applicant	Fujian Province Jiu Zhou Group
Product code	FMC
Device class	Class I
Decision date	Aug 29, 1990
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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PVC PATIENT EXAMINATION GLOVE

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