510(k) K883847 ยท KZE Injector, Fluid, Non-Electrically Powered
DERATA MEDI-JECTOR V
| Applicant | Derata Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 31, 1988 |
| Received | Sep 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883847
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.