510(k) K802103 ยท DSI Detector And Alarm, Arrhythmia
ECG RECALL & EDIT PRODUCT VERSION-A3601
| Applicant | General Electric Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 26, 1980 |
| Received | Sep 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802103
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.