510(k) K003908 ยท KZE Injector, Fluid, Non-Electrically Powered
SEROJET
| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Mar 8, 2001 |
| Received | Dec 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003908
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.