MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN

MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN is an FDA 510(k)-cleared medical device (K862227) manufactured by Hgm, Inc.. 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 August 18, 1986. Regulation: 8.