Documento fuente o registro público
FDA 510(k) K203272 — Alltest Pregnancy Rapid Combo Test Cassette
FDA 510(k) index record K203272. Device: Alltest Pregnancy Rapid Combo Test Cassette. Applicant as listed: Hangzhou AllTest Biotech Co., Ltd.. Decision date: 2022-01-31.
Fuente
"device_name": "Alltest Pregnancy Rapid Combo Test Cassette"
Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.
Review and references
Automated FDA record verification
2026-10-20
2026-10-31
professional use
FDA 510(k) public index record K203272.
Device name: Alltest Pregnancy Rapid Combo Test Cassette. Applicant as listed: Hangzhou AllTest Biotech Co., Ltd..
Decision date: 2022-01-31. Decision wording: Substantially Equivalent.
Product code: JHI. Regulation: 21 CFR 862.1155. Medical specialty: Clinical Chemistry.
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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