510(k) K960392 ยท LDM Instrumentation, High Pressure Liquid Chromatography
CDM
| Applicant | Bio-Rad, Hercules CA, US |
| Decision | Substantially Equivalent, Jul 8, 1996 |
| Received | Jan 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960392
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.