K-number	K821043
Device name	STERILE PATIENT EXAM. GLOVES
Applicant	Phoenix Glove Co.
Product code	FMC
Device class	Class I
Decision date	May 21, 1982
Decision	Substantially Equivalent
Regulation	880.6250

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View the full FDA submission: accessdata.fda.gov

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STERILE PATIENT EXAM. GLOVES

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