510(k) K912832 ยท LIO Device, Specimen Collection
BACTI-SWAB(TM) NPG
| Applicant | Remel Co., Lenexa KS, US |
| Decision | Substantially Equivalent, Aug 22, 1991 |
| Received | Jun 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912832
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.