510(k) K100225 ยท DQA Oximeter
PULSE OXIMETER MODEL P10
| Applicant | Mediana Co., Ltd., Echo OR, US |
| Decision | Substantially Equivalent, Feb 9, 2011 |
| Received | Jan 26, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100225
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.