510(k) K022164

Device
ZETA DIAGNOSTIC RETINAL IMAGING SYSTEM
Applicant
ZETA DEVELOPMENT LABORATORIES
510(k) number
K022164
Product code
HKI  
Decision
Substantially Equivalent (SESE)
Decision date
2002-07-26
Date received
2002-07-03
Regulation
886.1120
Classification name
Camera, Ophthalmic, Ac-powered
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
Yes

Applicant Contact#

Contact
MARK T FUKUHARA
Address
4990 Hillside Cir. Suite 400 El Dorado Hills CA US 95762 95762

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code HKI  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K251353Eyer 2Phelcom Technologies2026-01-16
K252120Fundus On Phone Non Mydriatic (FOP NM-10)Remidio Innovative Solutions Private Limited2025-12-12
K250770Optina-4C (MHRC-C1N)Optina Diagnostics, Inc.2025-09-04
K2436003nethra neo HD FA; 3nethra neo HDForus Health Pvt.Ltd2025-08-14
K250683Resolve Fundus CameraOptain Health, Inc.2025-04-30
K243664Sentinel CameraAi Optics2024-12-17
K242508Verily Numetric Retinal CameraVerily Life Sciences, LLC2024-12-09
K241049CANON Fundus Camera CR-10 (CR-10)Canon, Inc.2024-05-15
K231230Optina-4C (MHRC-C1N)Optina Diagnostics, Inc.2023-12-05
K230627Zilia Ocular FC (ZIL-10002)Zilia, Inc.2023-11-20
K223575Phoenix ICON, Phoenix ICON GONeolight, LLC2023-09-06
K223381iExaminer System with Panoptic PlusWelch Allyn, Inc.2023-03-15
K221329Eyer Retinal Camera NM-STDPhelcom Technologies2023-02-22
K221111Non-Mydriatic Retinal Camera NW500Topcon Corporation2022-08-29
K203500RetCam EnvisionNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)2021-04-13

Legacy Summary#

summary

FDA Review#

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