MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF) is an FDA 510(k)-cleared medical device (K940541) manufactured by Siemens Medical Solutions USA, 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 November 6, 1994. Regulation: 8.