meddevicedb.com FDA Device Reference

Disposable Grasping Forceps FG-52D/FG-54D

K250263 Class II Traditional
Decision Date
2025-03-31
Sponsor / Applicant
Olympus Medical Systems Corp.

Technical Specification

510(k) Submission ID K250263
Product Code KTI
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2025-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Grasping Forceps FG-52D/FG-54D received FDA 510(k) clearance under submission number K250263, sponsored by Olympus Medical Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2025-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code KTI and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.