
Directed Energy, Inc.
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MODEL 20-C WITH AN SA-20B/U OPT. ATTACH. HEMORRHO. is an FDA 510(k)-cleared medical device (K871029) manufactured by Directed Energy, 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 May 17, 1987. Regulation: 8.