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FDA 510(k)

Radiofrequency Generator System, Cura RF Electrode

K-Number: K240758 · 2024-12-11

ApplicantZhejiang Curaway Medical Technology Co., Ltd.
Decision Date2024-12-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Radiofrequency Generator System, Cura RF Electrode is a medical device manufactured by Zhejiang Curaway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-12-11 under approval number K240758. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Radiofrequency Generator System, Cura RF Electrode?

Radiofrequency Generator System, Cura RF Electrode is a medical device that received FDA 510(k) clearance on 2024-12-11. It is manufactured by Zhejiang Curaway Medical Technology Co., Ltd.. The 510(k) number is K240758.

When was Radiofrequency Generator System, Cura RF Electrode approved by the FDA?

Radiofrequency Generator System, Cura RF Electrode received FDA 510(k) clearance on 2024-12-11, under approval number K240758.

What company makes Radiofrequency Generator System, Cura RF Electrode?

Radiofrequency Generator System, Cura RF Electrode is manufactured by Zhejiang Curaway Medical Technology Co., Ltd..

What is the FDA product code for Radiofrequency Generator System, Cura RF Electrode?

The FDA product code for Radiofrequency Generator System, Cura RF Electrode is GEI.

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Other Devices by Zhejiang Curaway Medical Technology Co., Ltd.

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Official Source

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