510(k) K071610 ยท DQA Oximeter
MEDIAID PULSE OXIMETER M30 AND M34
| Applicant | Mediaid, Inc., Cerritos CA, US |
| Decision | Substantially Equivalent, Nov 5, 2007 |
| Received | Jun 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071610
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.