DERMALON,SURGILON,OPHTHALON,& OPHTHALMIC NYLON SUT

DERMALON,SURGILON,OPHTHALON,& OPHTHALMIC NYLON SUT is an FDA 510(k)-cleared medical device (K930586) manufactured by Davis & Geck, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1993. Regulation: 8.