510(k) K960373 ยท KZE Injector, Fluid, Non-Electrically Powered
BIOJECTOR 2000 MODEL 1B02000
| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Mar 5, 1997 |
| Received | Jan 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960373
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.