510(k) K861687 ยท KZE Injector, Fluid, Non-Electrically Powered
BIOJECTOR SYRINGE SYSTEM
| Applicant | Bioject, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Apr 23, 1987 |
| Received | May 2, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861687
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.