510(k) K851984 ยท KHO Fluorometer, For Clinical Use
LKB-WALLAC 1230 ARCUS FLUOROMETER
| Applicant | Lkb Instruments, Inc., Gaithersburg MD, US |
| Decision | Substantially Equivalent, May 24, 1985 |
| Received | May 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851984
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.