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FDA 510(k)

RetiCapture

K-Number: K173474 · 2018-07-27

ApplicantIlooda Co,., Ltd.
Decision Date2018-07-27
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RetiCapture is a medical device manufactured by Ilooda Co,., Ltd.. It received FDA 510(k) clearance on 2018-07-27 under approval number K173474. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RetiCapture?

RetiCapture is a medical device that received FDA 510(k) clearance on 2018-07-27. It is manufactured by Ilooda Co,., Ltd.. The 510(k) number is K173474.

When was RetiCapture approved by the FDA?

RetiCapture received FDA 510(k) clearance on 2018-07-27, under approval number K173474.

What company makes RetiCapture?

RetiCapture is manufactured by Ilooda Co,., Ltd..

What is the FDA product code for RetiCapture?

The FDA product code for RetiCapture is HKI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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