RECEPTAL ATS TRAUMA KGA1900L

RECEPTAL ATS TRAUMA KGA1900L is an FDA 510(k)-cleared medical device (K772196) manufactured by Sorensen Research. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 1977. Regulation: 8.