510(k) K850591 ยท GLZ Antigens, If, Toxoplasma Gondii
FIAX TOXO-M ANTIBODIES TEST KIT
| Applicant | Intl. Diagnostic Technology, San Jose CA, US |
| Decision | Substantially Equivalent, Apr 30, 1985 |
| Received | Feb 14, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850591
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.