510(k) K050734 ยท KZE Injector, Fluid, Non-Electrically Powered
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| Applicant | Bioject, Inc., Tualatin OR, US |
| Decision | Substantially Equivalent, Jun 3, 2005 |
| Received | Mar 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050734
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.