510(k) K803208 ยท DSI Detector And Alarm, Arrhythmia
SIRECUST 358
| Applicant | Siemens Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 27, 1981 |
| Received | Dec 18, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803208
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.