RetiCapture— 510(k) K173474

Substantially Equivalent

Ilooda Co,., Ltd.

FDA 510(k) clearance K173474 for RetiCapture, Substantially Equivalent on 2018-07-27. Applicant: Ilooda Co,., Ltd.. Device class: 2.

Clearance details

Applicant: Ilooda Co,., Ltd.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 2017-11-09
Decision date: 2018-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suwon-Si, KR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.