SFX-90 TABLE/SPOTFILMER W/FLUORICON L200

SFX-90 TABLE/SPOTFILMER W/FLUORICON L200 is an FDA 510(k)-cleared medical device (K801320) manufactured by General Electric Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1980. Regulation: 8.