510(k) K820122 ยท DRX Electrode, Electrocardiograph
PIONEER II BACK PLATE ELECTRODE
| Applicant | Life Science Instrumentation, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 1, 1982 |
| Received | Jan 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820122
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.