FIAX EB VCA-M TEST KIT

FIAX EB VCA-M TEST KIT is an FDA 510(k)-cleared medical device (K894932) manufactured by Whittaker Bioproducts, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 15, 1989. Regulation: 8.