MODIFICATION TO SYNCHRON SYSTEMS BENZODIAZEPINE REAGENT

MODIFICATION TO SYNCHRON SYSTEMS BENZODIAZEPINE REAGENT is an FDA 510(k)-cleared medical device (K023048) manufactured by Beckman Coulter, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 2002. Regulation: 8.