510(k) K890299 ยท DQA Oximeter
KONTRON PULSE OXIMETER 7840
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Mar 2, 1989 |
| Received | Jan 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890299
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.