510(k) K881883 ยท DQA Oximeter
SATLITE+/PB251+ PULSE OXIMETER
| Applicant | Datex Division Instrumentarium Corp., Helsinki, Finland, FI |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | May 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881883
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.