meddevicedb.com FDA Device Reference

SLIT LAMP SL-D4 (Type: LED)

K262637 Class II Traditional
Decision Date
2026-09-18
Sponsor / Applicant
Topcon Corporation

Technical Specification

510(k) Submission ID K262637
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 2026-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLIT LAMP SL-D4 (Type: LED) received FDA 510(k) clearance under submission number K262637, sponsored by Topcon Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2026-09-18.

Classification & Regulation

This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.