510(k) K790235 ยท KHO Fluorometer, For Clinical Use
SPECTROPHOTOMETER MODEL 3000
| Applicant | The Perkin-Elmer Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 15, 1979 |
| Received | Feb 1, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790235
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.