510(k) K800047 ยท KIE Apparatus, High Pressure Liquid Chromatography
LDC UVIII FIXED WAVELENGTH ULTRAVIOLET
| Applicant | Laboratory Data Control, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 21, 1980 |
| Received | Jan 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800047
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.