BioStar Single Use Transbronchial Aspiration Needle

BioStar Single Use Transbronchial Aspiration Needle is an FDA 510(k)-cleared medical device (K232038) manufactured by Broncus Medical, Inc.. 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 April 25, 2024. Regulation: 8.