ENDICOTT & BEAMAN SUPRA-TEC FACE MASK

ENDICOTT & BEAMAN SUPRA-TEC FACE MASK is an FDA 510(k)-cleared medical device (K881372) manufactured by Endicott & Beaman, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 7, 1988. Regulation: 8.