VECTRA MOBILE MAGNETIC RESONANCE IMAGING SYSTEM

VECTRA MOBILE MAGNETIC RESONANCE IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K931460) 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 March 3, 1994. Regulation: 8.