SERVOMED PULSE AMPLIFIER MODULE-206-

SERVOMED PULSE AMPLIFIER MODULE-206- is an FDA 510(k)-cleared medical device (K840523) manufactured by Litton Medical Electronics. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 28, 1984. Regulation: 8.