510(k) K884814 ยท GXY Electrode, Cutaneous
BIOTENS
| Applicant | Trekk Intl., Sausalito CA, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Nov 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884814
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.