510(k) K893905 ยท LIO Device, Specimen Collection
PATHODX(TM) CHLAMYDIA DIRECT SPECIMEN (PDCY1)
| Applicant | Diagnostic Products Corp., Los Angeles CA, US |
| Decision | Substantially Equivalent, Aug 3, 1989 |
| Received | May 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893905
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.