510(k) K832069 ยท LJK Antisera, If, Toxoplasma Gondii
TOXO IPA KIT IAN INDIRECT FLUORESCENT
| Applicant | Bionetic Laboratory Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1983 |
| Received | Jun 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832069
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.