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

3D Optical Coherence Tomography (3D OCT-1(type: Maestro2))

K Number: K233561 · Decision Apr 10, 2024
Classifications
1
FEI Numbers
29
Registration Numbers
30
Same Product Code
65
Applicant Total
13
Review Days
156

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Basic Information

Device Name
3D Optical Coherence Tomography (3D OCT-1(type: Maestro2))
K Number
K233561
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Topcon Corporation
Date Received
November 6, 2023
Decision Date
April 10, 2024
Product Code
OBO
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
OBO Tomography, Optical Coherence

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OBO), ordered by most recent decision date.

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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
K232828 IMAGEnet6 Ophthalmic Data System
K231222 3D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1(type: Maestro2)
K221111 Non-Mydriatic Retinal Camera NW500
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 →