# Daxor Corporation

- Location (FDA's records): Oak Ridge, TN
- FDA decisions: 4 (1997–2026): 4 510(k) clearances
- Product codes: JWO (3), FMF (1)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K251087: Blood Volume Analyzer (200) (2025), cited by 1
- K964406: Automated Multi-Point Blood Volume Analyzer (1997), cited by 1

## Recent decisions
- K261099: Blood Volume Analyzer (200) (Jun 18, 2026)
- K251087: Blood Volume Analyzer (200) (Aug 4, 2025)
- K970419: Daxor MAX100 Syringe (MAX100) (Dec 22, 1997)
- K964406: Automated Multi-Point Blood Volume Analyzer (Sep 25, 1997)

Source page: https://510kreport.com/company/daxor