510(k) K071672 ยท DQA Oximeter
SENTEC DIGITAL MONITORING SYSTEM
| Applicant | Sentec AG, Egale WI, US |
| Decision | Substantially Equivalent, Sep 12, 2007 |
| Received | Jun 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071672
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 17, 2016 | SenTec AG SDMS (SenTec Digital Monitoring System) Terminated |
LKD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.