510(k) K983684 ยท DQA Oximeter
DATEX-OHMEDA 3800+/3800P+ OR 3900/3900P PULSE OXIMETERS
| Applicant | Datex-Ohmeda, Inc., Louisville CO, US |
| Decision | Substantially Equivalent, Nov 6, 1998 |
| Received | Oct 20, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983684
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.