Last synced on 25 January 2026 at 3:41 am

BioSieveTM Multi-Drug Urine Test Panel; BioSieveTM Multi-Drug Urine Test Panel Rx

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233062
510(k) Type
Traditional
Applicant
Vivachek Biotech (Hangzhou) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
37 days
Submission Type
Summary

BioSieveTM Multi-Drug Urine Test Panel; BioSieveTM Multi-Drug Urine Test Panel Rx

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233062
510(k) Type
Traditional
Applicant
Vivachek Biotech (Hangzhou) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
37 days
Submission Type
Summary