Reprocessed Advisor HD Grid Mapping Catheter, Sensor Enabled

Reprocessed Advisor HD Grid Mapping Catheter, Sensor Enabled is an FDA 510(k)-cleared medical device (K200212) manufactured by Innovative Health, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 2020. Regulation: 8.