510(k) K901771 ยท DPS Electrocardiograph
SIEMENS SIRECUST 732, PATIENT MONITOR
| Applicant | Siemens Medical Electronics, Danvers MA, US |
| Decision | Substantially Equivalent, May 30, 1990 |
| Received | Apr 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901771
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.