Source document or public record
FDA 510(k) K242209 — UASure II Blood Uric Acid Monitoring System
FDA 510(k) index record K242209. Device: UASure II Blood Uric Acid Monitoring System. Applicant as listed: Apex BioTechnology Corp.. Decision date: 2025-04-04.
Source
"device_name": "UASure II Blood Uric Acid Monitoring System"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K242209.
Device name: UASure II Blood Uric Acid Monitoring System. Applicant as listed: Apex BioTechnology Corp..
Decision date: 2025-04-04. Decision wording: Substantially Equivalent.
Product code: PTC. Regulation: 21 CFR 862.1775. 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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