FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TRC-50DX RETINAL CAMERA

K Number: K123101 · Decision Jun 5, 2013
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
11
Review Days
244

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Basic Information

Device Name
TRC-50DX RETINAL CAMERA
K Number
K123101
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Topcon Medical Systems, Inc.
Date Received
October 4, 2012
Decision Date
June 5, 2013
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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K110489 SLIT LAMP SL-2G
K093313 SYNERGY
K083316 3D OCT-1000 MARK II OPTICAL COHERENCE TOMOGRAPHY SYSTEM
K072971 TOPCON 3D OCT-1000 OPTICAL COHERENCE TOMOGRAPHY SYSTEM FOR MEASUREMENT OF RETINAL THICKNESS
K031831 TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM
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