AIMI-Triage CXR PTX

AIMI-Triage CXR PTX is an FDA 510(k)-cleared medical device (K193300) manufactured by Radlogics, 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 7, 2020. Regulation: 8.