meddevicedb.com FDA Device Reference

Single-Use Biopsy Valve (MAJ-1555)

K251997 Class II Traditional
Decision Date
2025-09-25
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K251997
Product Code OCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2025-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Single-Use Biopsy Valve (MAJ-1555) received FDA 510(k) clearance under submission number K251997, 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 2025-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code OCX and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.