510(k) K994085 ยท DHA System, Test, Human Chorionic Gonadotropin
IMMULITE TURBO HCG, MODELS LSKCG1, LSKCG5
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Jan 28, 2000 |
| Received | Dec 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994085
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.