Source document or public record
FDA 510(k) K261280 — BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test Panel
FDA 510(k) index record K261280. Device: BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test Panel. Applicant as listed: Vivachek Biotech (Hangzhou) Co., Ltd.. Decision date: 2026-05-22.
Source
"device_name": "BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test Panel"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K261280.
Device name: BioSieve Multi-Drug Urine Test Panel;BioSieve Multi-Drug Urine Home Test Panel. Applicant as listed: Vivachek Biotech (Hangzhou) Co., Ltd..
Decision date: 2026-05-22. Decision wording: Substantially Equivalent.
Product code: NFT. Regulation: 21 CFR 862.3100. Medical specialty: Clinical Toxicology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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