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FDA 510(k)

Aqua Medical RF Vapor Ablation System

K-Number: K241271 · 2024-12-12

Decision Date2024-12-12
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Aqua Medical RF Vapor Ablation System is a medical device manufactured by Aqua Medical, Inc.. It received FDA 510(k) clearance on 2024-12-12 under approval number K241271. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aqua Medical RF Vapor Ablation System?

Aqua Medical RF Vapor Ablation System is a medical device that received FDA 510(k) clearance on 2024-12-12. It is manufactured by Aqua Medical, Inc.. The 510(k) number is K241271.

When was Aqua Medical RF Vapor Ablation System approved by the FDA?

Aqua Medical RF Vapor Ablation System received FDA 510(k) clearance on 2024-12-12, under approval number K241271.

What company makes Aqua Medical RF Vapor Ablation System?

Aqua Medical RF Vapor Ablation System is manufactured by Aqua Medical, Inc..

What is the FDA product code for Aqua Medical RF Vapor Ablation System?

The FDA product code for Aqua Medical RF Vapor Ablation System is KNS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.