510(k) K871748 ยท DRX Electrode, Electrocardiograph
THE BUDDY SYSTEM W/OPTIONAL ECG ELECTRODE
| Applicant | The Buddy Systems, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 10, 1987 |
| Received | May 5, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871748
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.