P2020 MOBILE C-ARM IMAGE INTENSIFIER

P2020 MOBILE C-ARM IMAGE INTENSIFIER is an FDA 510(k)-cleared medical device (K874905) manufactured by Photo Medic Equipment, 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 February 25, 1988. Regulation: 8.