WIRELESS STANDARD PROBE, DYNAMIC REFERENCE FRAME (DRF)

WIRELESS STANDARD PROBE, DYNAMIC REFERENCE FRAME (DRF) is an FDA 510(k)-cleared medical device (K982364) manufactured by Radionics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 1998. Regulation: 8.