EzRay M (Model: VMX-P300)
K-Number: K203667 · 2021-02-02
Device Summary
Frequently Asked Questions
What is the EzRay M (Model: VMX-P300)?
EzRay M (Model: VMX-P300) is a medical device that received FDA 510(k) clearance on 2021-02-02. The listed applicant is VATECH Co., Ltd.. The 510(k) number is K203667.
When did EzRay M (Model: VMX-P300) receive FDA 510(k) clearance?
EzRay M (Model: VMX-P300) received FDA 510(k) clearance on 2021-02-02, under 510(k) number K203667.
Who is the listed applicant for EzRay M (Model: VMX-P300)?
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 M (Model: VMX-P300)?
The FDA product code for EzRay M (Model: VMX-P300) is IZL.
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: IZL)
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.