510(k) K881820 ยท DQA Oximeter
EDENTEC MODEL 2800/2801 OXIMETER/PULSE OXIMETER
| Applicant | Edentec Corp., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | Apr 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881820
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.