Source document or public record
FDA 510(k) K253188 — CoaguChek XS Plus System
FDA 510(k) index record K253188. Device: CoaguChek XS Plus System. Applicant as listed: Roche Diagnostics. Decision date: 2025-10-24.
Source
"device_name": "CoaguChek XS 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 K253188.
Device name: CoaguChek XS Plus System. Applicant as listed: Roche Diagnostics.
Decision date: 2025-10-24. Decision wording: Substantially Equivalent.
Product code: GJS. Regulation: 21 CFR 864.7750. Medical specialty: Hematology.
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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