CoreDx™ Pulmonary Mini-Forceps

CoreDx™ Pulmonary Mini-Forceps is an FDA 510(k)-cleared medical device (K183085) manufactured by Boston Scientific Corporation. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 7, 2019. Regulation: 8.