Veloxion System
K-Number: K230205 · 2023-02-24
Device Summary
Frequently Asked Questions
What is the Veloxion System?
Veloxion System is a medical device that received FDA 510(k) clearance on 2023-02-24. It is manufactured by Corinth Medtech, Inc.. The 510(k) number is K230205.
When was Veloxion System approved by the FDA?
Veloxion System received FDA 510(k) clearance on 2023-02-24, under approval number K230205.
What company makes Veloxion System?
Veloxion System is manufactured by Corinth Medtech, Inc..
What is the FDA product code for Veloxion System?
The FDA product code for Veloxion System is FJL.
Other Devices by Corinth Medtech, Inc.
Related Devices (Code: FJL)
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.