CERAMATEC MAXCELL AND CAG GALVANIC OXYGEN SENSORS

CERAMATEC MAXCELL AND CAG GALVANIC OXYGEN SENSORS is an FDA 510(k)-cleared medical device (K972992) manufactured by Ceramatec, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 29, 1998. Regulation: 8.