510(k) K871826 ยท DQA Oximeter
PB VIDEO DISPLAY TO PB251 PULSE OXIMETER UPGRADE
| Applicant | Datex Division Instrumentarium Corp., Helsinki, Finland, FI |
| Decision | Substantially Equivalent, Jun 29, 1987 |
| Received | May 11, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871826
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.