510(k) K013293 ยท FMI Needle, Hypodermic, Single Lumen
NIPRO HYPODERMIC NEEDLE
| Applicant | Nipro Medical Corp., Lexington KY, US |
| Decision | Substantially Equivalent, Dec 14, 2001 |
| Received | Oct 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013293
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.