510(k) K993757 ยท DSI Detector And Alarm, Arrhythmia
SOLAR 7/8000
| Applicant | General Electric Medical Systems Information Techn, Milwaukee WI, US |
| Decision | Substantially Equivalent, Mar 23, 2000 |
| Received | Nov 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993757
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.