510(k) K881939 ยท DPS Electrocardiograph
SIRECUST 1280/1281 & 960/961 PATIENT MONITORS
| Applicant | Siemens Medical Electronics, Danvers MA, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | May 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881939
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.