EzRay Air W
K-Number: K163705 · 2017-01-24
ApplicantVATECH Co., Ltd.
Decision Date2017-01-24
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
EzRay Air W is a medical device manufactured by VATECH Co., Ltd.. It received FDA 510(k) clearance on 2017-01-24 under approval number K163705. 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 W?
EzRay Air W is a medical device that received FDA 510(k) clearance on 2017-01-24. It is manufactured by VATECH Co., Ltd.. The 510(k) number is K163705.
When was EzRay Air W approved by the FDA?
EzRay Air W received FDA 510(k) clearance on 2017-01-24, under approval number K163705.
What company makes EzRay Air W?
EzRay Air W is manufactured by VATECH Co., Ltd..
What is the FDA product code for EzRay Air W?
The FDA product code for EzRay Air W 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.