510(k) K890502 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
MICROLITE TUBE LUMINOMETER #011-902-0000
| Applicant | Dynatech Laboratories, Inc., Chantilly VA, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Feb 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890502
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.