510(k) K083148 ยท DRX Electrode, Electrocardiograph
TELECTRODE WET GEL ECG ELECTRODE
| Applicant | Bio Protech, Inc., Woonju-Si, Gangwon-Do, KR |
| Decision | Substantially Equivalent, Nov 7, 2008 |
| Received | Oct 24, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083148
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.