510(k) K884614 ยท DQA Oximeter
EDENTEC MODEL 2000W OPTION S CARDIO-RESP. PROCESS.
| Applicant | Edentec Corp., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Feb 1, 1989 |
| Received | Nov 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884614
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.