Versus Catheter (VS110-8B)
K-Number: K241851 · 2024-11-25
Device Summary
Frequently Asked Questions
What is the Versus Catheter (VS110-8B)?
Versus Catheter (VS110-8B) is a medical device that received FDA 510(k) clearance on 2024-11-25. It is manufactured by Liquet Medical, Inc.. The 510(k) number is K241851.
When was Versus Catheter (VS110-8B) approved by the FDA?
Versus Catheter (VS110-8B) received FDA 510(k) clearance on 2024-11-25, under approval number K241851.
What company makes Versus Catheter (VS110-8B)?
Versus Catheter (VS110-8B) is manufactured by Liquet Medical, Inc..
What is the FDA product code for Versus Catheter (VS110-8B)?
The FDA product code for Versus Catheter (VS110-8B) is QEY.
Related Clinical Trials
Other Devices by Liquet Medical, Inc.
Related Devices (Code: QEY)
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.