GYROSCAN T5 MAGNETIC RESONANCE DIAGNOSTIC DEVICE

GYROSCAN T5 MAGNETIC RESONANCE DIAGNOSTIC DEVICE is an FDA 510(k)-cleared medical device (K890789) manufactured by Philips Medical Systems North America, 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 April 27, 1989. Regulation: 8.