CO2 Laser Bronchoscope Set

K870063 is the FDA 510(k) clearance record for CO2 LASER BRONCHOSCOPE SET, a class II device, cleared for Tti Medical on 1987-03-09 under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)). FDA's definition for product code EOQ reads: "A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the...". FDA records list 9 510(k) clearances for Tti Medical, from 1987-03-05 to 1995-05-31. As of 2026-09-10, FDA records show no recalls naming K870063.