510(k) K781771 ยท KIE Apparatus, High Pressure Liquid Chromatography
DETECTOR, MODEL 79875A, VARIABLE
| Applicant | Hewlett-Packard Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 20, 1978 |
| Received | Oct 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781771
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.