510(k) K883009 ยท FMI Needle, Hypodermic, Single Lumen
NON-CORING NEEDLES
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Oct 4, 1988 |
| Received | Jul 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883009
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.