PULSE KLYSTRON AMPLIFIER (L-5822-00)

PULSE KLYSTRON AMPLIFIER (L-5822-00) is an FDA 510(k)-cleared medical device (K951142) manufactured by Litton Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 1995. Regulation: 8.