Last synced on 25 November 2022 at 11:04 pm

Sclerotherapy Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212668
510(k) Type
Traditional
Applicant
Zhejiang Chuangxiang Medical Technology Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/23/2022
Days to Decision
184 days
Submission Type
Summary

Sclerotherapy Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212668
510(k) Type
Traditional
Applicant
Zhejiang Chuangxiang Medical Technology Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/23/2022
Days to Decision
184 days
Submission Type
Summary