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FDA 510(k)

Vantage Titan 3T, MRT-3010, V2.5

K-Number: K191128 · 2019-06-26

Decision Date2019-06-26
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Vantage Titan 3T, MRT-3010, V2.5 is a medical device manufactured by Canon Medical Systems Corporation. It received FDA 510(k) clearance on 2019-06-26 under approval number K191128. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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