510(k) K964406 ยท JWO Device, Blood Volume Measuring
AUTOMATED MULTI-POINT BLOOD VOLUME ANALYZER
| Applicant | Daxor Corporation, New York NY, US |
| Decision | Substantially Equivalent, Sep 25, 1997 |
| Received | Nov 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964406
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.