FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Non-Mydriatic Retinal Camera NW500

K Number: K221111 · Decision Aug 29, 2022
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
13
Review Days
136

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Basic Information

Device Name
Non-Mydriatic Retinal Camera NW500
K Number
K221111
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Topcon Corporation
Date Received
April 15, 2022
Decision Date
August 29, 2022
Product Code
HKI
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HKI Camera, Ophthalmic, Ac-Powered

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Other Clearances by Topcon Corporation

K Number Device Name
K253039 AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIA
K241081 3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1 (type: Maestro2); IMAGEnet6 Ophthalmic Data System
K233561 3D Optical Coherence Tomography (3D OCT-1(type: Maestro2))
K232828 IMAGEnet6 Ophthalmic Data System
K231222 3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1(type: Maestro2)
K173119 DRI OCT Triton
K171370 IMAGEnet 6 Ophthalmic Data System
K170164 3D OCT-1 Maestro
K161972 Slit Lamp SL-D301
K161509 3D OCT-1 Maestro
Search all 13 clearances from Topcon Corporation →