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TRC-NW400 NON-MYDRIATIC RETINAL CAMERA

K141481 Class II Traditional
Decision Date
2014-09-17
Sponsor / Applicant
Topcon Corporation

Technical Specification

510(k) Submission ID K141481
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 2014-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRC-NW400 NON-MYDRIATIC RETINAL CAMERA received FDA 510(k) clearance under submission number K141481, 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 2014-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code HKI and 21 CFR 886.1120, within the Ophthalmic review panel as a Class II device.