510(k) K844244 ยท KZE Injector, Fluid, Non-Electrically Powered
DERATA MEDI-JECTOR PRO
| Applicant | Derata Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 5, 1985 |
| Received | Nov 1, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844244
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.