SHERIDAN YSI/SONATEMP

SHERIDAN YSI/SONATEMP is an FDA 510(k)-cleared medical device (K841098) manufactured by Sheridan Catheter 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 April 29, 1984. Regulation: 8.