EzRay M (Model: VMX-P300)
K-Number: K203667 · 2021-02-02
ApplicantVATECH Co., Ltd.
Decision Date2021-02-02
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EzRay M (Model: VMX-P300) is a medical device manufactured by VATECH Co., Ltd.. It received FDA 510(k) clearance on 2021-02-02 under approval number K203667. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by VATECH Co., Ltd.. The 510(k) number is K203667.
When was EzRay M (Model: VMX-P300) approved by the FDA?
EzRay M (Model: VMX-P300) received FDA 510(k) clearance on 2021-02-02, under approval number K203667.
What company makes EzRay M (Model: VMX-P300)?
EzRay M (Model: VMX-P300) is manufactured by VATECH Co., Ltd..
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 Devices by VATECH Co., Ltd.
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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.