510(k) K880672 ยท DQA Oximeter
SENTINEL PULSE OXIMETER
| Applicant | Sentinel Monitoring Technologies, Ltd., Indianapolis IN, US |
| Decision | Substantially Equivalent, May 6, 1988 |
| Received | Feb 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880672
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.