K-number	K890701
Device name	ENDOTHELIAL GROWTH MEDIUM (EGM)
Applicant	Clonetics Corp.
Product code	KIT
Device class	Class I
Decision date	Feb 24, 1989
Decision	Substantially Equivalent
Regulation	864.2220

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View the full FDA submission: accessdata.fda.gov

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ENDOTHELIAL GROWTH MEDIUM (EGM)

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