FDA 510(k) Applications Submitted by DAXOR CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K964406 | 11/04/1996 | AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER | DAXOR CORPORATION |
| K970419 | 02/04/1997 | DAXOR MAX100 SYRINGE (MAX100) | DAXOR CORPORATION |
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