Source document or public record
FDA 510(k) K252475 — ABL90 FLEX PLUS System
FDA 510(k) index record K252475. Device: ABL90 FLEX PLUS System. Applicant as listed: Radiometer Medicals Aps. Decision date: 2026-05-01.
Source
"device_name": "ABL90 FLEX PLUS System"
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 K252475.
Device name: ABL90 FLEX PLUS System. Applicant as listed: Radiometer Medicals Aps.
Decision date: 2026-05-01. 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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