510(k) K820217 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
LKB-WALLACE 1251 LUMINOMETER
| Applicant | Lkb Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 12, 1982 |
| Received | Jan 26, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820217
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.