SERVOMED OXCARDIORE SPIROGRAPH 324/111

SERVOMED OXCARDIORE SPIROGRAPH 324/111 is an FDA 510(k)-cleared medical device (K840832) manufactured by Litton Medical Electronics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 1984. Regulation: 8.