Nordica PV Cryo Mapping Catheter

Nordica PV Cryo Mapping Catheter is an FDA 510(k)-cleared medical device (K233900) manufactured by Synaptic Medical Corporation. 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 5, 2024. Regulation: 8.