Rhino-Laryngo Fiberscope Olympus ENF-GP2

K181240 is the FDA 510(k) clearance record for Rhino-Laryngo Fiberscope Olympus ENF-GP2, a class II device, cleared for Olympus Medical Systems Corp. on 2018-10-04 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 186 510(k) clearances for Olympus Medical Systems Corp., from 2004-12-09 to 2026-07-31. As of 2026-09-10, FDA records show one recall naming K181240.