510(k) K082052 ยท DQA Oximeter
MASIMO RAINBOW SET RADCHECK PULSE CO-OXIMETER, RADCHECK, RAD 57 SPOT CHECK
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 10, 2008 |
| Received | Jul 21, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082052
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.