510(k) K842368 ยท GHM Test, Sickle Cell
SICKLE CELL REAGENT SET
| Applicant | Livonia Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1984 |
| Received | Jun 15, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842368
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.