510(k) K100617 ยท DQA Oximeter
MASIMO RESPONSABLE OXIMETRY SENSORS MODEL S2-25/25D; S2-20/20D
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, May 28, 2010 |
| Received | Mar 4, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100617
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.