Mural Perinatal Surveillance

Mural Perinatal Surveillance is an FDA 510(k)-cleared medical device (K220732) manufactured by Ge Medical Systems Information Technologies, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 2022. Regulation: 8.