510(k) K882485 ยท LIO Device, Specimen Collection
DIVERSI-KIT
| Applicant | Intl. Cancer Screening Laboratories, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | Jun 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882485
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.