510(k) K831765 ยท FMI Needle, Hypodermic, Single Lumen
HERAPIN LOCK FLUSH SOLUTION USE KIT
| Applicant | Smith & Nephew, Mpl Division, Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 12, 1983 |
| Received | Jun 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831765
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.