Documento fuente o registro público
FDA 510(k) K261099 — Blood Volume Analyzer (200)
FDA 510(k) index record K261099. Device: Blood Volume Analyzer (200). Applicant as listed: Daxor Corporation. Decision date: 2026-06-18.
Fuente
"device_name": "Blood Volume Analyzer (200)"
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Review and references
Automated FDA record verification
2026-10-20
2026-10-22
professional use
FDA 510(k) public index record K261099.
Device name: Blood Volume Analyzer (200). Applicant as listed: Daxor Corporation.
Decision date: 2026-06-18. Decision wording: Substantially Equivalent.
Product code: JWO. Regulation: 21 CFR 864.5950. 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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