510(k) K970419 ยท FMF Syringe, Piston
DAXOR MAX100 SYRINGE (MAX100)
| Applicant | Daxor Corporation, Knoxville TN, US |
| Decision | Substantially Equivalent, Dec 22, 1997 |
| Received | Feb 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970419
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.