510(k) K071642 ยท DQA Oximeter
MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER
| Applicant | Mediaid, Inc., Cerritos CA, US |
| Decision | Substantially Equivalent, May 2, 2008 |
| Received | Jun 18, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071642
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.