Fnl-10P, Fiber Nasoparhyngoscope

K951196 is the FDA 510(k) clearance record for FNL-10P, FIBER NASOPARHYNGOSCOPE, a class II device, cleared for Pentax Precision Instrument Corp. on 1995-04-07 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 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 K951196.