510(k) K151341 ยท FMI Needle, Hypodermic, Single Lumen
Turbo High-Flow Non-coring Needle
| Applicant | Norfolk Medical, Skokie IL, US |
| Decision | Substantially Equivalent, Aug 20, 2015 |
| Received | May 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151341
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.