DEVICE, FEMALE INCONTINENCE

DEVICE, FEMALE INCONTINENCE is an FDA 510(k)-cleared medical device (K781863) manufactured by Eschmann Bros. & Walsh , Ltd.. 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 November 5, 1978. Regulation: 8.