510(k) K052474 ยท FMI Needle, Hypodermic, Single Lumen
NIPRO HYPODERMIC NEEDLE
| Applicant | Nipro Medical Corp., Lexington KY, US |
| Decision | Substantially Equivalent, Nov 10, 2005 |
| Received | Sep 9, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052474
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.