Vantage Titan 3T, MRT-3010, V2.5
K-Number: K191128 · 2019-06-26
Device Summary
Frequently Asked Questions
What is the Vantage Titan 3T, MRT-3010, V2.5?
Vantage Titan 3T, MRT-3010, V2.5 is a medical device that received FDA 510(k) clearance on 2019-06-26. It is manufactured by Canon Medical Systems Corporation. The 510(k) number is K191128.
When was Vantage Titan 3T, MRT-3010, V2.5 approved by the FDA?
Vantage Titan 3T, MRT-3010, V2.5 received FDA 510(k) clearance on 2019-06-26, under approval number K191128.
What company makes Vantage Titan 3T, MRT-3010, V2.5?
Vantage Titan 3T, MRT-3010, V2.5 is manufactured by Canon Medical Systems Corporation.
What is the FDA product code for Vantage Titan 3T, MRT-3010, V2.5?
The FDA product code for Vantage Titan 3T, MRT-3010, V2.5 is LNH.
Other Devices by Canon Medical Systems Corporation
Related Devices (Code: LNH)
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.