GelPOINT V-Path Vaginal Access System

GelPOINT V-Path Vaginal Access System is an FDA 510(k)-cleared medical device (K220969) manufactured by Applied Medical Resources Corporation. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 15, 2022. Regulation: 8.