PULSE KLYSTRON AMPLIFIFER (L-5822-90)

PULSE KLYSTRON AMPLIFIFER (L-5822-90) is an FDA 510(k)-cleared medical device (K951143) 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 18, 1995. Regulation: 8.