510(k) K834553 ยท FMI Needle, Hypodermic, Single Lumen
INTRADISCAL THERAPY TRAY
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Mar 6, 1984 |
| Received | Dec 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834553
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.