Viz ANEURYSM, Viz ANX

Viz ANEURYSM, Viz ANX is an FDA 510(k)-cleared medical device (K213319) manufactured by Viz. Ai, 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 February 17, 2022. Regulation: 8.