510(k) K062268 ยท DQA Oximeter
MASIMO SET SPO2 MODULE FOR PHILIPS AND M3001A MULTI-MEASUREMENT SERVER OPTION A03
| Applicant | Philips Medical Systems North America Co., Andover MA, US |
| Decision | Substantially Equivalent, Oct 18, 2006 |
| Received | Aug 7, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062268
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.