SHERIDAN/ENDO-PAK

SHERIDAN/ENDO-PAK is an FDA 510(k)-cleared medical device (K842635) 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 July 24, 1984. Regulation: 8.