Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter

Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter is an FDA 510(k)-cleared medical device (K190127) 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 August 22, 2019. Regulation: 8.