510(k) K770988 ยท DRX Electrode, Electrocardiograph
FOAM ECG ELECTRODE, 2060 AND 2061
| Applicant | Cardio-Dynamics Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 14, 1977 |
| Received | May 31, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770988
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.