510(k) K882216 ยท DRX Electrode, Electrocardiograph
SYNCOR (R) MODEL S-801 ECG ELECTRODE
| Applicant | Lectec Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jul 20, 1988 |
| Received | May 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882216
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.