510(k) K800556 ยท KIE Apparatus, High Pressure Liquid Chromatography
DIFFERENTIAL REFRACTIVE INDEX DETECTOR
| Applicant | Hewlett-Packard Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 25, 1980 |
| Received | Mar 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800556
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.