510(k) K822942 ยท KHO Fluorometer, For Clinical Use
INNOTRON FLUORIMETER SERIES ONE-10
| Applicant | Innotron of Oregon, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 9, 1982 |
| Received | Oct 4, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822942
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.