510(k) K931383 ยท LIO Device, Specimen Collection
ZINC PVA
| Applicant | Remel Co., Lenexa KS, US |
| Decision | Substantially Equivalent, Jun 15, 1993 |
| Received | Mar 18, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931383
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.