VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM MUMPS IGG ASSA

VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM MUMPS IGG ASSA is an FDA 510(k)-cleared medical device (K923903) manufactured by Biomerieux Vitek, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 8, 1993. Regulation: 8.