PREAMPLIFIER MODULE, EKG RESPIRATION

PREAMPLIFIER MODULE, EKG RESPIRATION is an FDA 510(k)-cleared medical device (K790304) manufactured by Abbott Medical Electronics Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 1979. Regulation: 8.