K261099
- 510(k) number
- K261099
- Device name
- Blood Volume Analyzer (200)
- Applicant
- Daxor Corporation TN · US
- Product code
- JWO — Device, Blood Volume Measuring
- Decision date
- 2026-06-18
- Date received
- 2026-04-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Hematology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K261099.pdf
Official FDA record: K261099
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.