510(k) K041280 ยท KZE Injector, Fluid, Non-Electrically Powered
HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500
| Applicant | Felton International, Inc., Lee'S Summit MO, US |
| Decision | Substantially Equivalent, Jun 24, 2004 |
| Received | May 13, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041280
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.