FDA 510(k)

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter

Numéro K : K232505 · 2024-05-30

DemandeurZhejiang Curaway Medical Technology Co., Ltd.

Date de décision2024-05-30

Code produitGEI

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Curaway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-05-30 under 510(k) number K232505. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter?

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter is a medical device that received FDA 510(k) clearance on 2024-05-30. The listed applicant is Zhejiang Curaway Medical Technology Co., Ltd.. The 510(k) number is K232505.

When did Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter receive FDA 510(k) clearance?

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter received FDA 510(k) clearance on 2024-05-30, under 510(k) number K232505.

Who is the listed applicant for Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter?

The FDA 510(k) record lists Zhejiang Curaway Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter?

The FDA product code for Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter is GEI.

Essais cliniques associés

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Source officielle

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