LYFO KWIK(TM) RUS KIT

LYFO KWIK(TM) RUS KIT is an FDA 510(k)-cleared medical device (K870731) manufactured by Micro-Bio-Logics. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 16, 1987. Regulation: 8.