510(k) K831361 ยท JHJ Agglutination Method, Human Chorionic Gonadotropin
BETA-PREG
| Applicant | Catheter Technology Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jun 2, 1983 |
| Received | Apr 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831361
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.