510(k) K840799 ยท LIO Device, Specimen Collection
V.D.T.-GONORRHEA TEST KIT
| Applicant | M.G. Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 7, 1984 |
| Received | Feb 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840799
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.