510(k) K926131 ยท KHO Fluorometer, For Clinical Use
OPUS MAGNUM ANALYZER
| Applicant | Pb Diagnostic Systems, Inc., Westwood MA, US |
| Decision | Substantially Equivalent, Jun 7, 1993 |
| Received | Dec 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926131
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.