VIRATEST-DIA(TM) MEASLES (RUBEOLA)

VIRATEST-DIA(TM) MEASLES (RUBEOLA) is an FDA 510(k)-cleared medical device (K910290) manufactured by Virus Reference Laboratory, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 17, 1992. Regulation: 8.