meddevicedb.com FDA Device Reference

Coronis Fusion 4MP (MDCC-4630); Coronis Fusion 6MP (MDCC-6630)

K262412 Class II Special
Decision Date
2026-10-02
Sponsor / Applicant
Barco NV

Technical Specification

510(k) Submission ID K262412
Product Code PGY
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2026-10-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Coronis Fusion 4MP (MDCC-4630); Coronis Fusion 6MP (MDCC-6630) received FDA 510(k) clearance under submission number K262412, sponsored by Barco NV. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code PGY and 21 CFR 892.2050, within the Radiology review panel as a Class II device.