Merge Hemo, Model RCSV2

Merge Hemo, Model RCSV2 is an FDA 510(k)-cleared medical device (K233326) manufactured by Merge Healthcare Incorporated. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 20, 2024. Regulation: 8.