
Utah Medical Products, Inc.
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FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC is an FDA 510(k)-cleared medical device (K952981) manufactured by Utah Medical Products, 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 August 27, 1995. Regulation: 8.