510(k) K800201 ยท DRX Electrode, Electrocardiograph
ESOPHAGEAL PILL-ELECTRODE
| Applicant | Arzbaecher & Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 26, 1980 |
| Received | Jan 30, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800201
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.