
Peregrine Surgical , Ltd.
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PEREGRINE FIBER OPTIC MULTI-FUNCTION MANIPULATOR is an FDA 510(k)-cleared medical device (K980797) manufactured by Peregrine Surgical , Ltd.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 1998. Regulation: 8.