CEREGLIDE 92 Intermediate Catheter

CEREGLIDE 92 Intermediate Catheter is an FDA 510(k)-cleared medical device (K230726) manufactured by Cerenovus, 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 November 28, 2023. Regulation: 8.