Xenf-Tp Rhino-Laryngofiberscope, Its Acessories and Ancillary Equipment

K013591 is the FDA 510(k) clearance record for XENF-TP RHINO-LARYNGOFIBERSCOPE, ITS ACESSORIES AND ANCILLARY EQUIPMENT, a class II device, cleared for Olympus Optical Co., Ltd. on 2001-12-26 under FDA product code EOB (Nasopharyngoscope (Flexible Or Rigid)). FDA's definition for product code EOB reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 48 510(k) clearances for Olympus Optical Co., Ltd., from 1996-11-29 to 2003-10-16. As of 2026-09-10, FDA records show no recalls naming K013591.