UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I is an FDA 510(k)-cleared medical device (K981213) 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 June 30, 1998. Regulation: 8.