MASTER SCREEN PNUEMO

MASTER SCREEN PNUEMO is an FDA 510(k)-cleared medical device (K933839) manufactured by Erich Jaeger, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 6, 1994. Regulation: 8.