EzVu Visual Vasopressor injector (EV-19)

FDA 510(k) K241595 · Veol Medical Technologies Pvt , Ltd.

Substantially Equivalent

510(k) numberK241595

Submission

Device name
EzVu Visual Vasopressor injector (EV-19)
Applicant
Veol Medical Technologies Pvt , Ltd.
Navi Mumbai, IN
Received
June 3, 2024
Decision date
February 27, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBK – Endoscopic Injection Needle, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.

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Questions and answers

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

EzVu Visual Vasopressor injector (EV-19) (K241595) received a 510(k) decision of Substantially Equivalent on February 27, 2025, 269 days after the submission was received.

What is the product code of K241595?

The FDA product code is FBK – Endoscopic Injection Needle, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.