Documento fuente o registro público
FDA 510(k) K223187 — HemosIL Liquid Anti-Xa
FDA 510(k) index record K223187. Device: HemosIL Liquid Anti-Xa. Applicant as listed: Instrumentation Laboratory CO. Decision date: 2023-06-23.
Fuente
"device_name": "HemosIL Liquid Anti-Xa"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-29
professional use
FDA 510(k) public index record K223187.
Device name: HemosIL Liquid Anti-Xa. Applicant as listed: Instrumentation Laboratory CO.
Decision date: 2023-06-23. Decision wording: Substantially Equivalent.
Product code: QLU. Regulation: 21 CFR 864.7295. 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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