REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA

REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA is an FDA 510(k)-cleared medical device (K894259) manufactured by Washington Regulatory Services. 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 March 4, 1990. Regulation: 8.