Documento fuente o registro público
FDA 510(k) K200913 — Clearblue® Early Digital Pregnancy Test
FDA 510(k) index record K200913. Device: Clearblue® Early Digital Pregnancy Test. Applicant as listed: Spd Swiss Precision Diagnostics GmbH. Decision date: 2021-08-13.
Fuente
"device_name": "Clearblue® Early Digital Pregnancy Test"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K200913.
Device name: Clearblue® Early Digital Pregnancy Test. Applicant as listed: Spd Swiss Precision Diagnostics GmbH.
Decision date: 2021-08-13. Decision wording: Substantially Equivalent.
Product code: LCX. 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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