Documento fuente o registro público
FDA 510(k) K203562 — Finetest Lite Blood Glucose Monitoring System
FDA 510(k) index record K203562. Device: Finetest Lite Blood Glucose Monitoring System. Applicant as listed: Osang Healthcare Co. , Ltd.. Decision date: 2021-07-13.
Fuente
"device_name": "Finetest Lite Blood Glucose Monitoring System"
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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 K203562.
Device name: Finetest Lite Blood Glucose Monitoring System. Applicant as listed: Osang Healthcare Co. , Ltd..
Decision date: 2021-07-13. Decision wording: Substantially Equivalent.
Product code: NBW. Regulation: 21 CFR 862.1345. 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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