510(k) K901209 ยท DQA Oximeter
MODEL 90489 PULSE OXIMETER MODULE
| Applicant | Spacelabs, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Apr 30, 1990 |
| Received | Mar 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901209
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.