Visualase V2 MRI-guided Laser Ablation System (9736422)
K-Number: K250307 · 2025-05-29
Device Summary
Frequently Asked Questions
What is the Visualase V2 MRI-guided Laser Ablation System (9736422)?
Visualase V2 MRI-guided Laser Ablation System (9736422) is a medical device that received FDA 510(k) clearance on 2025-05-29. It is manufactured by Medtronic Navigation. The 510(k) number is K250307.
When was Visualase V2 MRI-guided Laser Ablation System (9736422) approved by the FDA?
Visualase V2 MRI-guided Laser Ablation System (9736422) received FDA 510(k) clearance on 2025-05-29, under approval number K250307.
What company makes Visualase V2 MRI-guided Laser Ablation System (9736422)?
Visualase V2 MRI-guided Laser Ablation System (9736422) is manufactured by Medtronic Navigation.
What is the FDA product code for Visualase V2 MRI-guided Laser Ablation System (9736422)?
The FDA product code for Visualase V2 MRI-guided Laser Ablation System (9736422) is ONO.
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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.