510(k) K890791 ยท DPS Electrocardiograph
SIEMENS SIRECUST 730 PATIENT MONITOR
| Applicant | Siemens Medical Electronics, Danvers MA, US |
| Decision | Substantially Equivalent, May 2, 1989 |
| Received | Feb 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890791
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.