510(k) K890033 ยท DQA Oximeter
MODEL 8700 PULSE OXIMETER
| Applicant | Nonin Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 6, 1989 |
| Received | Jan 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890033
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.