Wingman 14, Wingman 14C, Wingman 18, Wingman 35

Wingman 14, Wingman 14C, Wingman 18, Wingman 35 is an FDA 510(k)-cleared medical device (K193596) manufactured by Reflow Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 19, 2020. Regulation: 8.