JWO
- Product code
- JWO
- Device name
- Device, Blood Volume Measuring
- Device class
- Class 2
- 21 CFR
- 21 CFR 864.5950
- Medical specialty
- Hematology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 3 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K261099 | 2026-06-18 | Daxor Corporation | Blood Volume Analyzer (200) | |
| K251087 | 2025-08-04 | Daxor Corporation | Blood Volume Analyzer (200) | FDA |
Official FDA classification page: JWO
Classification and pathway per current FDA publications. Data from openFDA (CC0).