meddevicedb.com FDA Device Reference

DFC-1024 & DFC-512 DIGITAL IMAGING SYSTEM

K913929 Class II Traditional
Decision Date
1991-11-27
Sponsor / Applicant
Ophthalmic Imaging Systems

Technical Specification

510(k) Submission ID K913929
Product Code HKI
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1120
Decision Date 1991-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DFC-1024 & DFC-512 DIGITAL IMAGING SYSTEM received FDA 510(k) clearance under submission number K913929, sponsored by Ophthalmic Imaging Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1991-11-27.

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.