Endoscopes for Sinus Surgery

K874215 is the FDA 510(k) clearance record for ENDOSCOPES FOR SINUS SURGERY, a class II device, cleared for Richards Medical Co., Inc. on 1988-01-04 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 71 510(k) clearances for Richards Medical Co., Inc., from 1983-09-29 to 1990-06-25. As of 2026-09-10, FDA records show no recalls naming K874215.