510(k) K895425 ยท DQA Oximeter
MINIMON 7137B PATIENT MONITOR
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Sep 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895425
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.