RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA

RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA is an FDA 510(k)-cleared medical device (K910304) manufactured by Vitek Systems, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 25, 1991. Regulation: 8.