REMEL RIM STREPTOCOCCUS GROUPING LATEX AGGLUTINATION TEST

REMEL RIM STREPTOCOCCUS GROUPING LATEX AGGLUTINATION TEST is an FDA 510(k)-cleared medical device (K942093) manufactured by Medical Diagnostic Technologies, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 27, 1994. Regulation: 8.