510(k) K001572 ยท FMI Needle, Hypodermic, Single Lumen
NEOLUS NEEDLE
| Applicant | Terumo Europe N.V., Leuven, BE |
| Decision | Substantially Equivalent, Aug 14, 2000 |
| Received | May 22, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001572
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.