510(k) K024018 ยท KZE Injector, Fluid, Non-Electrically Powered
AVANT GUARDIAN 101
| Applicant | Avant Medical Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, Jan 17, 2003 |
| Received | Dec 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024018
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.