510(k) K780031 ยท KHO Fluorometer, For Clinical Use
FLUORESCENCE DETECTOR MODEL 420
| Applicant | Waters Assoc., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 20, 1978 |
| Received | Jan 9, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780031
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.