PEREGRINE WIDE ANGLE LIGHT PIPE

PEREGRINE WIDE ANGLE LIGHT PIPE is an FDA 510(k)-cleared medical device (K940393) manufactured by Peregrine Surgical , Ltd.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 1, 1994. Regulation: 8.