510(k) K100815 ยท DQA Oximeter
OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIMETER MODEL MD300C316
| Applicant | Oxypulse, Mesa AZ, US |
| Decision | Substantially Equivalent, Jun 16, 2010 |
| Received | Mar 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100815
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.