510(k) K920888 ยท KHO Fluorometer, For Clinical Use
MICROLITE MICROTITER PLATE LUMINOMETER ML2200
| Applicant | Dynatech Laboratories, Inc., Chantilly VA, US |
| Decision | Substantially Equivalent, Mar 19, 1992 |
| Received | Feb 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920888
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.