510(k) K973899 ยท FMI Needle, Hypodermic, Single Lumen
UNIFINE PENTIPS
| Applicant | Owen Mumford USA, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Dec 4, 1997 |
| Received | Oct 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973899
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.