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FDA 510(k)

EzVu Visual Vasopressor injector (EV-19)

K-Number: K241595 · 2025-02-27

Decision Date2025-02-27
Product CodeFBK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EzVu Visual Vasopressor injector (EV-19) is a medical device manufactured by Veol Medical Technologies Pvt , Ltd.. It received FDA 510(k) clearance on 2025-02-27 under approval number K241595. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EzVu Visual Vasopressor injector (EV-19)?

EzVu Visual Vasopressor injector (EV-19) is a medical device that received FDA 510(k) clearance on 2025-02-27. It is manufactured by Veol Medical Technologies Pvt , Ltd.. The 510(k) number is K241595.

When was EzVu Visual Vasopressor injector (EV-19) approved by the FDA?

EzVu Visual Vasopressor injector (EV-19) received FDA 510(k) clearance on 2025-02-27, under approval number K241595.

What company makes EzVu Visual Vasopressor injector (EV-19)?

EzVu Visual Vasopressor injector (EV-19) is manufactured by Veol Medical Technologies Pvt , Ltd..

What is the FDA product code for EzVu Visual Vasopressor injector (EV-19)?

The FDA product code for EzVu Visual Vasopressor injector (EV-19) is FBK.

Other Devices by Veol Medical Technologies Pvt , Ltd.

Related Devices (Code: FBK)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.