PEREGRINE WET SET, MODEL PD400.00

PEREGRINE WET SET, MODEL PD400.00 is an FDA 510(k)-cleared medical device (K990518) manufactured by Peregrine Surgical , Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 1999. Regulation: 8.