510(k) K070193 ยท DQA Oximeter
ENVITEC OXIPEN PULSE OXIMETER AND ACCESSORIES
| Applicant | Envitec-Wismar GmbH, Egale WI, US |
| Decision | Substantially Equivalent, May 2, 2007 |
| Received | Jan 22, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070193
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.