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FDA 510(k)

Finiff System

K-Number: K242688 · 2024-12-20

ApplicantSkingrab Co., Ltd.
Decision Date2024-12-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Finiff System is a medical device manufactured by Skingrab Co., Ltd.. It received FDA 510(k) clearance on 2024-12-20 under approval number K242688. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Finiff System?

Finiff System is a medical device that received FDA 510(k) clearance on 2024-12-20. It is manufactured by Skingrab Co., Ltd.. The 510(k) number is K242688.

When was Finiff System approved by the FDA?

Finiff System received FDA 510(k) clearance on 2024-12-20, under approval number K242688.

What company makes Finiff System?

Finiff System is manufactured by Skingrab Co., Ltd..

What is the FDA product code for Finiff System?

The FDA product code for Finiff System is GEI.

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Official Source

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