510(k) K780122 ยท KHO Fluorometer, For Clinical Use
HTSH RIA
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Feb 3, 1978 |
| Received | Jan 23, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780122
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.