SENSORMEDICS MODEL 6200 AUTOBOX DL

SENSORMEDICS MODEL 6200 AUTOBOX DL is an FDA 510(k)-cleared medical device (K923989) manufactured by Sensor Medics Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 8, 1993. Regulation: 8.