BAKER DIAG. ULTRARATE CHLORIDE KIT

BAKER DIAG. ULTRARATE CHLORIDE KIT is an FDA 510(k)-cleared medical device (K802080) manufactured by J.T. Baker Chemical Co.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 1980. Regulation: 8.