NEO-MED DLS-1100

NEO-MED DLS-1100 is an FDA 510(k)-cleared medical device (K954931) manufactured by Neo-Laboratories, LLC. 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 December 17, 1995. Regulation: 8.