meddevicedb.com FDA Device Reference

ClearTip TBNA Type

K251478 Class II Traditional
Decision Date
2026-04-16
Sponsor / Applicant
Finemedix Co., Ltd.

Technical Specification

510(k) Submission ID K251478
Product Code KTI
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2026-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ClearTip TBNA Type received FDA 510(k) clearance under submission number K251478, sponsored by Finemedix Co., Ltd.. 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 2026-04-16.

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.