510(k) K994384 ยท KZE Injector, Fluid, Non-Electrically Powered
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| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Jun 22, 2000 |
| Received | Dec 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994384
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.