Rology Teleradiology Platform (v.1.22.1103)

Rology Teleradiology Platform (v.1.22.1103) is an FDA 510(k)-cleared medical device (K231385) manufactured by Rology, 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 September 19, 2023. Regulation: 8.