K-number	K942923
Device name	CERES 900C & CERES UV900C
Applicant	Bio-Tek Instruments, Inc.
Product code	JJQ
Device class	Class I
Decision date	Feb 6, 1995
Decision	Substantially Equivalent
Regulation	862.2300

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View the full FDA submission: accessdata.fda.gov

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CERES 900C & CERES UV900C

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