MERITEC-STREP GROUP A BETA-HEMOLYTIC

MERITEC-STREP GROUP A BETA-HEMOLYTIC is an FDA 510(k)-cleared medical device (K831599) manufactured by Meridian Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 10, 1983. Regulation: 8.