REFLAB SYSTEM PACK LIQUID CO2 REAGENT

REFLAB SYSTEM PACK LIQUID CO2 REAGENT is an FDA 510(k)-cleared medical device (K926320) manufactured by Medical Analysis Systems, Inc.. 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 February 2, 1993. Regulation: 8.