Last synced on 24 January 2025 at 11:04 pm

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232505
510(k) Type
Traditional
Applicant
Zhejiang CuraWay Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/30/2024
Days to Decision
286 days
Submission Type
Summary

Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232505
510(k) Type
Traditional
Applicant
Zhejiang CuraWay Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/30/2024
Days to Decision
286 days
Submission Type
Summary