Source document or public record
FDA 510(k) K242244 — Viewer+
FDA 510(k) index record K242244. Device: Viewer+. Applicant as listed: Lumea, Inc.. Decision date: 2025-03-14.
Source
"device_name": "Viewer+"
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 K242244.
Device name: Viewer+. Applicant as listed: Lumea, Inc..
Decision date: 2025-03-14. Decision wording: Substantially Equivalent.
Product code: QKQ. Regulation: 21 CFR 864.3700. Medical specialty: Pathology.
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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