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Harmony Referral System with Harmony OCT Viewer (Octave)

K253893 Class II Traditional
Decision Date
2026-06-04
Sponsor / Applicant
Topcon Healthcare Solutions EMEA Oy

Technical Specification

510(k) Submission ID K253893
Product Code NFJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2026-06-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Harmony Referral System with Harmony OCT Viewer (Octave) received FDA 510(k) clearance under submission number K253893, sponsored by Topcon Healthcare Solutions EMEA Oy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-06-04.

Classification & Regulation

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