510(k) K221111

Device
Non-Mydriatic Retinal Camera NW500
Applicant
Topcon Corporation
510(k) number
K221111
Product code
HKI
Decision
Substantially Equivalent (SESE)
Decision date
2022-08-29
Date received
2022-04-15
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
N

Related Records

Applicant Contact

Contact
Ryota Kitawaki
Address
75-1 Hasunuma-Cho Itabashi-Ku JP 174-8580 174-8580

FDA Registration Numbers

Source Documents

510(k) summary PDF

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