K-number	K792211
Device name	SPECIMAN CUP & EMESIS BASIN
Applicant	General Clinical Plastics Corp.
Product code	FMH
Device class	Class I
Decision date	Nov 16, 1979
Decision	Substantially Equivalent
Regulation	864.3250

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View the full FDA submission: accessdata.fda.gov

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SPECIMAN CUP & EMESIS BASIN

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