510(k) K801289 ยท LCP Assay, Glycosylated Hemoglobin
LEECO GLYCO-HEMOGLOBIN DIAG. TEST KIT
| Applicant | Leeco Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 30, 1980 |
| Received | May 30, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801289
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.