510(k) K840044 ยท JJO Flame Emission Photometer For Clinical Use
SDI PREPAX DILUKIT 29-1000
| Applicant | Scientific Distributors, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 9, 1984 |
| Received | Jan 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840044
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.