510(k) K874249 ยท FMI Needle, Hypodermic, Single Lumen
BIFURCATED NEEDLE
| Applicant | Allergy Laboratories of Ohio, Inc., Columbus OH, US |
| Decision | Substantially Equivalent, Nov 3, 1987 |
| Received | Oct 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874249
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.