510(k) K043359 ยท DQA Oximeter
4100 PATIENT OXIMETER MODULE
| Applicant | Nonin Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jan 7, 2005 |
| Received | Dec 6, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043359
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.