MINI 6800 DIGITAL MOBILE C-ARM

MINI 6800 DIGITAL MOBILE C-ARM is an FDA 510(k)-cleared medical device (K992506) manufactured by Ge Dec Medical Systems. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 1999. Regulation: 8.