FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

RetiCapture

K Number: K173474 · Decision Jul 27, 2018
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
16
Review Days
260

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Basic Information

Device Name
RetiCapture
K Number
K173474
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ilooda Co,., Ltd.
Date Received
November 9, 2017
Decision Date
July 27, 2018
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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