Documento fuente o registro público
FDA 510(k) K213486 — GLP systems Track
FDA 510(k) index record K213486. Device: GLP systems Track. Applicant as listed: Abbott Laboratories. Decision date: 2022-03-10.
Fuente
"device_name": "GLP systems Track"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-31
professional use
FDA 510(k) public index record K213486.
Device name: GLP systems Track. Applicant as listed: Abbott Laboratories.
Decision date: 2022-03-10. Decision wording: Substantially Equivalent.
Product code: JGS. Regulation: 21 CFR 862.1665. 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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