Voyant Open Sealer-Divider Device

Voyant Open Sealer-Divider Device is an FDA 510(k)-cleared medical device (K143517) manufactured by Applied Medical Resources. 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 March 26, 2015. Regulation: 8.