VITRIFICATION KIT & VITRIFICATION WARMING KIT

VITRIFICATION KIT & VITRIFICATION WARMING KIT is an FDA 510(k)-cleared medical device (K073522) manufactured by Sage In-Vitro Fertilization, 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 October 9, 2008. Regulation: 8.