510(k) K060093 ยท DQE Catheter, Oximeter, Fiber-Optic
PRESEP OLIGON OXIMETRY CATHETERS
| Applicant | Edwards Lifesciences, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Apr 28, 2006 |
| Received | Jan 12, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060093
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.