510(k) K930074 ยท JGJ Photometric Method, Magnesium
IN-VITRO DIAGNOSTIC REAGENT SET
| Applicant | Horizon Diagnostics, Inc., Jackson MI, US |
| Decision | Substantially Equivalent, May 11, 1993 |
| Received | Jan 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930074
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.