COMBISON 530D WITH POWER DOPPLER MODE

COMBISON 530D WITH POWER DOPPLER MODE is an FDA 510(k)-cleared medical device (K974813) manufactured by Medison America, 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 September 28, 1998. Regulation: 8.