Source document or public record
FDA 510(k) K223093 — Aptiva APS IgG Reagent; Aptiva APS IgM Reagent
FDA 510(k) index record K223093. Device: Aptiva APS IgG Reagent; Aptiva APS IgM Reagent. Applicant as listed: Inova Diagnostics, Inc.. Decision date: 2024-12-17.
Source
"device_name": "Aptiva APS IgG Reagent; Aptiva APS IgM Reagent"
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 K223093.
Device name: Aptiva APS IgG Reagent; Aptiva APS IgM Reagent. Applicant as listed: Inova Diagnostics, Inc..
Decision date: 2024-12-17. Decision wording: Substantially Equivalent.
Product code: MID. Regulation: 21 CFR 866.5660. Medical specialty: Immunology.
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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