K-number	K860282
Device name	RPMI 1640 W/GLUTAMINE W/HEPES
Applicant	Newport Biosystems, Inc.
Product code	KIT
Device class	Class I
Decision date	Feb 5, 1986
Decision	Substantially Equivalent
Regulation	864.2220

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View the full FDA submission: accessdata.fda.gov

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RPMI 1640 W/GLUTAMINE W/HEPES

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