510(k) K851632 ยท DRW Adaptor, Lead Switching, Electrocardiograph
PCX-100 PATIENT INPUT LEADWIRE
| Applicant | Eaton Medical Group, Eaton MI, US |
| Decision | Substantially Equivalent, Nov 8, 1985 |
| Received | Apr 18, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851632
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.