510(k) K903934 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
GEN-PROBE LUMINOMETER-LEADER 50
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 27, 1990 |
| Received | Aug 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903934
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.