Broncho Fiberscope Fb-19C

K832492 is the FDA 510(k) clearance record for BRONCHO FIBERSCOPE FB-19C, a class II device, cleared for Pentax Precision Instrument Corp. on 1983-09-20 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 67 510(k) clearances for Pentax Precision Instrument Corp., from 1979-12-10 to 2004-06-09. As of 2026-09-10, FDA records show no recalls naming K832492.