510(k) K853705 ยท DRX Electrode, Electrocardiograph
BOMED-EEA
| Applicant | Bomed Medical Mfr., Ltd., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 13, 1986 |
| Received | Sep 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853705
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.