
Stiefel Research Institute, Inc.
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L.C.S. 2000 SYSTEM is an FDA 510(k)-cleared medical device (K914591) manufactured by Stiefel Research Institute, 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 January 13, 1992. Regulation: 8.