IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE

IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE is an FDA 510(k)-cleared medical device (K914171) manufactured by Tech Intl. Co.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 17, 1991. Regulation: 8.