L/U ARM - NEURO - VASCULAR #B5080B

L/U ARM - NEURO - VASCULAR #B5080B is an FDA 510(k)-cleared medical device (K791830) 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 October 25, 1979. Regulation: 8.