RM Electrode (RMH 23-01)

RM Electrode (RMH 23-01) is an FDA 510(k)-cleared medical device (K232273) manufactured by Retmap, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2023. Regulation: 8.