SURVEYOR I, RESPIRATORY COMPUTER SYSTEM

SURVEYOR I, RESPIRATORY COMPUTER SYSTEM is an FDA 510(k)-cleared medical device (K801526) manufactured by The Devilbiss Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1980. Regulation: 8.