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Daxor Corporation
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
4
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K251087
Blood Volume Analyzer (200)
August 4, 2025
K970419
DAXOR MAX100 SYRINGE (MAX100)
December 22, 1997
K964406
AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER
September 25, 1997