RMS 111F RESPIRATORY MONITORING SYSTEM

RMS 111F RESPIRATORY MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K800086) manufactured by The Perkin-Elmer 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 May 7, 1980. Regulation: 8.