RECEPTAL ATS MEDIASTINAL LINER

RECEPTAL ATS MEDIASTINAL LINER is an FDA 510(k)-cleared medical device (K772280) 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 January 2, 1978. Regulation: 8.