510(k) K920867 ยท DRX Electrode, Electrocardiograph
EME MP3000 MONITORING AND DIAGNOSTIC RESTING ECG
| Applicant | Electro Medical Equipment Co., Inc., Baton Rouge LA, US |
| Decision | Substantially Equivalent, Apr 10, 1992 |
| Received | Feb 25, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920867
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.