510(k) K884430 ยท DHA System, Test, Human Chorionic Gonadotropin
SERUM HCG MICROASSAY
| Applicant | Diamedix Corp., Miami FL, US |
| Decision | Substantially Equivalent, Dec 9, 1988 |
| Received | Oct 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884430
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.