510(k) K894625 ยท LKI Antisera, Fluorescent, Chlamydia Spp.
CHLAMYDIA (LGV-1)
| Applicant | Bion Ent., Ltd., Park Ridge IL, US |
| Decision | Substantially Equivalent, Aug 15, 1989 |
| Received | Jul 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894625
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.