510(k) K831977 ยท DRX Electrode, Electrocardiograph
C TEC SERIES 9000 E.C.G. ELECTRODE
| Applicant | Speywood Medical, Ltd., Walker MI, US |
| Decision | Substantially Equivalent, Sep 9, 1983 |
| Received | Jun 20, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831977
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.