510(k) K113469 ยท FMI Needle, Hypodermic, Single Lumen
NIPRO HUBER INFUSION, EXCEL HUBER NEEDLE
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Oct 18, 2012 |
| Received | Nov 22, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113469
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.