510(k) K810103 ยท DRX Electrode, Electrocardiograph
ADULT ECG ELECTRODE #60-0724
| Applicant | Aspen Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 29, 1981 |
| Received | Jan 16, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810103
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.