510(k) K890323 ยท DSI Detector And Alarm, Arrhythmia
MAX-1 (EXERCISE ELECTROCARDIOGRAPH)
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 16, 1989 |
| Received | Jan 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890323
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.