Cannulated Biopsy Forceps

K926430 is the FDA 510(k) clearance record for CANNULATED BIOPSY FORCEPS, a class II device, cleared for Thomasville Medical Assoc. on 1993-03-26 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 33 510(k) clearances for Thomasville Medical Assoc., from 1993-02-16 to 1994-02-28. As of 2026-09-10, FDA records show no recalls naming K926430.