The Trust
K-Number: K222688 · 2024-08-09
ApplicantGenoss Co., Ltd.
Decision Date2024-08-09
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
The Trust is a medical device manufactured by Genoss Co., Ltd.. It received FDA 510(k) clearance on 2024-08-09 under approval number K222688. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the The Trust?
The Trust is a medical device that received FDA 510(k) clearance on 2024-08-09. It is manufactured by Genoss Co., Ltd.. The 510(k) number is K222688.
When was The Trust approved by the FDA?
The Trust received FDA 510(k) clearance on 2024-08-09, under approval number K222688.
What company makes The Trust?
The Trust is manufactured by Genoss Co., Ltd..
What is the FDA product code for The Trust?
The FDA product code for The Trust is EKX.
Other Devices by Genoss Co., Ltd.
Related Devices (Code: EKX)
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.