SENSI-TOUCH EPIDURAL ANESTHESIA FILTER

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER is an FDA 510(k)-cleared medical device (K954525) manufactured by Sherwood Medical Co.. 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 18, 1996. Regulation: 8.