
Stellartech Research Corp.
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STELLARTECH COAGULATION SYSTEM, MODELS (1100C-115 & 1100C-230) is an FDA 510(k)-cleared medical device (K032062) manufactured by Stellartech Research Corp.. 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 July 28, 2003. Regulation: 8.