510(k) K042301 ยท GXY Electrode, Cutaneous
PROTENS ELECTRODE
| Applicant | Bio Protech, Inc., Crofton MD, US |
| Decision | Substantially Equivalent, Sep 3, 2004 |
| Received | Aug 25, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042301
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.