Medline ReNewal Reprocessed St. Jude Medical Livewire Steerable Electrophysiology Catheter

Medline ReNewal Reprocessed St. Jude Medical Livewire Steerable Electrophysiology Catheter is an FDA 510(k)-cleared medical device (K221067) manufactured by Surgical Instrument Service and Savings, 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 May 30, 2023. Regulation: 8.