EzRay Air 2 Wall (Model: VEX-S350W)
K-Number: K223058 · 2022-10-26
ApplicantVATECH Co., Ltd.
Decision Date2022-10-26
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
EzRay Air 2 Wall (Model: VEX-S350W) is a medical device manufactured by VATECH Co., Ltd.. It received FDA 510(k) clearance on 2022-10-26 under approval number K223058. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EzRay Air 2 Wall (Model: VEX-S350W)?
EzRay Air 2 Wall (Model: VEX-S350W) is a medical device that received FDA 510(k) clearance on 2022-10-26. It is manufactured by VATECH Co., Ltd.. The 510(k) number is K223058.
When was EzRay Air 2 Wall (Model: VEX-S350W) approved by the FDA?
EzRay Air 2 Wall (Model: VEX-S350W) received FDA 510(k) clearance on 2022-10-26, under approval number K223058.
What company makes EzRay Air 2 Wall (Model: VEX-S350W)?
EzRay Air 2 Wall (Model: VEX-S350W) is manufactured by VATECH Co., Ltd..
What is the FDA product code for EzRay Air 2 Wall (Model: VEX-S350W)?
The FDA product code for EzRay Air 2 Wall (Model: VEX-S350W) is EHD.
Other Devices by VATECH Co., Ltd.
Related Devices (Code: EHD)
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.