510(k) K131021 ยท DQA Oximeter
PULSE OXIMETER
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 11, 2013 |
| Received | Apr 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131021
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.