510(k) K040259 ยท DQA Oximeter
MASIMO SET INTELLIVUE PULSE OXIMETER MODULE
| Applicant | Masimo Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 22, 2004 |
| Received | Feb 4, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040259
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.