510(k) K093853 ยท DQA Oximeter
SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 4, 2010 |
| Received | Dec 16, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093853
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.