PERITONE DISPOSAL SHEATH - RUBBER AND VINYL

PERITONE DISPOSAL SHEATH - RUBBER AND VINYL is an FDA 510(k)-cleared medical device (K860552) manufactured by Laurie Ann Kaiser, Ph.D.. 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 April 16, 1986. Regulation: 8.