MAGNETOM P8 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

MAGNETOM P8 MAGNETIC RESONANCE DIAGNOSTIC DEVICE is an FDA 510(k)-cleared medical device (K911991) 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 July 18, 1991. Regulation: 8.