Halo Single-Loop Microsnare Kit

Halo Single-Loop Microsnare Kit is an FDA 510(k)-cleared medical device (K200963) manufactured by Argon Medical Devices, 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 January 4, 2021. Regulation: 8.