REAGENT, RUSSEL VIPER VENOM - LA CONFIRM

REAGENT, RUSSEL VIPER VENOM - LA CONFIRM is an FDA 510(k)-cleared medical device (K132076) manufactured by Dsrv, Inc.. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 9, 2014. Regulation: 8.