meddevicedb.com FDA Device Reference

OEC One CFD

K253269 Class II Traditional
Decision Date
2025-11-26
Sponsor / Applicant
Ge Hualun Medical Systems Co. , Ltd.

Technical Specification

510(k) Submission ID K253269
Product Code OXO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2025-11-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OEC One CFD received FDA 510(k) clearance under submission number K253269, sponsored by Ge Hualun Medical Systems Co. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-11-26.

Classification & Regulation

This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.