510(k) K901060 ยท DQA Oximeter
EDENTEC MODEL 2000W SYSTEM 700 MONITOR
| Applicant | Edentec Corp., Eden Prairie MN, US |
| Decision | Substantially Equivalent, May 15, 1990 |
| Received | Mar 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901060
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.