510(k) K124041 ยท DQA Oximeter
NBM-200MP
| Applicant | Orsense, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Oct 17, 2013 |
| Received | Dec 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K124041
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.