510(k) K983203 ยท GGT Assay, Erythropoietin
IMMULITE EPO, MODEL #'S LKEPZ & LKEP1
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jul 12, 1999 |
| Received | Sep 14, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983203
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.