510(k) K962625 ยท KZE Injector, Fluid, Non-Electrically Powered
VITAJET
| Applicant | Vitajet Corp., Laguna Hills CA, US |
| Decision | Substantially Equivalent, Dec 10, 1996 |
| Received | Jul 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962625
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.