SERIES 6600 DIGITAL MOBILE C-ARM

SERIES 6600 DIGITAL MOBILE C-ARM is an FDA 510(k)-cleared medical device (K951765) 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 May 10, 1995. Regulation: 8.