510(k) K893793 ยท GXY Electrode, Cutaneous
TENZCARE ELECTRODE 6862
| Applicant | 3M Company, Cottae Grove MN, US |
| Decision | Substantially Equivalent, Nov 27, 1989 |
| Received | May 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893793
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.