
Peregrine Surgical , Ltd.
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PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10 is an FDA 510(k)-cleared medical device (K031023) 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 June 26, 2003. Regulation: 8.

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