510(k) K872219 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
GEN-PROBE (R) LUMINOMETER - LEADER (TM)
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 21, 1987 |
| Received | Jun 12, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872219
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.