510(k) K871278 ยท LJP Antiserum, Fluorescent, Chlamydia Trachomatis
MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT
| Applicant | California Integrated Diagnostics, Inc., Berkeley CA, US |
| Decision | Substantially Equivalent, Apr 8, 1987 |
| Received | Mar 31, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871278
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.