LINQ II™ Insertable Cardiac Monitor (LNQ22)

LINQ II™ Insertable Cardiac Monitor (LNQ22) is an FDA 510(k)-cleared medical device (K233320) manufactured by Medtronic, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 2023. Regulation: 8.