MED-TEC REDI-FOAM

MED-TEC REDI-FOAM is an FDA 510(k)-cleared medical device (K951808) manufactured by Medtec, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 5, 1995. Regulation: 8.