DIGIRAD 2020TC SPECT IMAGING SYSTEM

DIGIRAD 2020TC SPECT IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K982855) manufactured by Digirad Corp.. 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 3, 1998. Regulation: 8.