ValvuloPro Valvuloplasty Balloon Catheter
K-Number: K240967 · 2024-07-31
Device Summary
Frequently Asked Questions
What is the ValvuloPro Valvuloplasty Balloon Catheter?
ValvuloPro Valvuloplasty Balloon Catheter is a medical device that received FDA 510(k) clearance on 2024-07-31. It is manufactured by Dongguan TT Medical, Inc.. The 510(k) number is K240967.
When was ValvuloPro Valvuloplasty Balloon Catheter approved by the FDA?
ValvuloPro Valvuloplasty Balloon Catheter received FDA 510(k) clearance on 2024-07-31, under approval number K240967.
What company makes ValvuloPro Valvuloplasty Balloon Catheter?
ValvuloPro Valvuloplasty Balloon Catheter is manufactured by Dongguan TT Medical, Inc..
What is the FDA product code for ValvuloPro Valvuloplasty Balloon Catheter?
The FDA product code for ValvuloPro Valvuloplasty Balloon Catheter is OZT.
Related Clinical Trials
Related PubMed Literature
Other Devices by Dongguan TT Medical, Inc.
Related Devices (Code: OZT)
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.