L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is an FDA 510(k)-cleared medical device (K230669) manufactured by Argon Medical Devices. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 29, 2023. Regulation: 8.