510(k) K862610 ยท FMI Needle, Hypodermic, Single Lumen
ULTRA-VUE SPINAL TYPE BIOPSY NEEDLE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Feb 4, 1987 |
| Received | Jul 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862610
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.