510(k) K992238 ยท DQA Oximeter
MASIMO SET RADICAL PULSE OXIMETER, LNOP-ADT, LNOP-PDT, LNOP-NEO, LNOP-NEO PT, LNOP-DCI, PATIENT CABLE (PC04, PC08, PC12)
| Applicant | Masimo Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 8, 1999 |
| Received | Jul 2, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992238
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.