QUANTA LITE RUBEOLA (MEASLES) IGG

QUANTA LITE RUBEOLA (MEASLES) IGG is an FDA 510(k)-cleared medical device (K971620) manufactured by Inova Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 21, 1997. Regulation: 8.