510(k) K020003 ยท DRX Electrode, Electrocardiograph
ELECTROCARDIOGRAPH (ECG) ELECTRODE, NON-STERILE
| Applicant | Bio Protech, Inc., Sparks NV, US |
| Decision | Substantially Equivalent, Nov 7, 2002 |
| Received | Jan 2, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020003
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.