510(k) K110893 ยท DQA Oximeter
VTRUST FINGER TYPE PULSE OXIMETER
| Applicant | Taidoc Technology Corporation, Taipei County, TW |
| Decision | Substantially Equivalent, Nov 22, 2011 |
| Received | Mar 30, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110893
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.