CENTRIA SYSTEM

Analyzer, Chemistry, Centrifugal, For Clinical Use

UNION CARBIDE CORP.

The following data is part of a premarket notification filed by Union Carbide Corp. with the FDA for Centria System.

Pre-market Notification Details

Device IDK790550
510k NumberK790550
Device Name:CENTRIA SYSTEM
ClassificationAnalyzer, Chemistry, Centrifugal, For Clinical Use
Applicant UNION CARBIDE CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJJG  
CFR Regulation Number862.2140 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-03-20
Decision Date1979-05-07

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