MODEL 2300 GENERAL PURPOSE SUCTION PUMP

MODEL 2300 GENERAL PURPOSE SUCTION PUMP is an FDA 510(k)-cleared medical device (K941527) manufactured by Product & Educational Services. 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 May 17, 1994. Regulation: 8.