510(k) K895839 ยท LJP Antiserum, Fluorescent, Chlamydia Trachomatis
PATHODX CHLAMYDIA CULTURE CONFIRMATION PKCC1
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Feb 1, 1990 |
| Received | Oct 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895839
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.