510(k) K013711 ยท LIO Device, Specimen Collection
BACTI-SWAB DRY
| Applicant | Remel Co., Lenexa KS, US |
| Decision | Substantially Equivalent, Nov 26, 2001 |
| Received | Nov 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013711
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.