Advisor HD Grid Mapping Catheter, Sensor Enabled

Advisor HD Grid Mapping Catheter, Sensor Enabled is an FDA 510(k)-cleared medical device (K172393) manufactured by St. Jude Medical, 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 April 22, 2018. Regulation: 8.