EzRay Air W
K-Number: K163705 · 2017-01-24
Device Summary
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. The listed applicant is VATECH Co., Ltd.. The 510(k) number is K163705.
When did EzRay Air W receive FDA 510(k) clearance?
EzRay Air W received FDA 510(k) clearance on 2017-01-24, under 510(k) number K163705.
Who is the listed applicant for EzRay Air W?
The FDA 510(k) record lists VATECH Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EzRay Air W?
The FDA product code for EzRay Air W is EHD.
Other records listing VATECH Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EHD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.