meddevicedb.com FDA Device Reference

Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)

K250187 Class II Traditional
Decision Date
2025-10-07
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K250187
Product Code KGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2025-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U) received FDA 510(k) clearance under submission number K250187, sponsored by Olympus Medical Systems Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2025-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code KGE and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.