510(k) K790837 ยท DSI Detector And Alarm, Arrhythmia
ARRHYTHMIA II CARDULE
| Applicant | Spacelabs, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 16, 1979 |
| Received | Apr 30, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790837
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.