510(k) K802452 ยท GMM Antigens, Iha, Toxoplasma Gondii
TOXOTEST-MT EIKEN KIT
| Applicant | Syn-Kit, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 18, 1980 |
| Received | Oct 8, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802452
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.