510(k) K874414 ยท FMI Needle, Hypodermic, Single Lumen
HYPODERMIC NEEDLES, SINGLE LUMEN
| Applicant | Harbor Medical Devices, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Jan 14, 1988 |
| Received | Oct 28, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874414
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.