510(k) K873533 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE
| Applicant | Medical Electronics Laboratories, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jan 29, 1988 |
| Received | Sep 1, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873533
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.