510(k) K911124 ยท DQA Oximeter
503 PULSE OXIMETER
| Applicant | Criticare Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 7, 1991 |
| Received | Mar 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911124
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.