510(k) K831610 ยท FMI Needle, Hypodermic, Single Lumen
INTRADISCAL THERAPY NEEDLE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Jul 12, 1983 |
| Received | May 19, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831610
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.