510(k) K192603 ยท GXZ Electrode, Needle
Spes Medica Subdermal Needle Electrodes
| Applicant | Spes Medica Srl, Battipaglia (Sa), IT |
| Decision | Substantially Equivalent, Nov 22, 2019 |
| Received | Sep 20, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192603
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.