510(k) K790316 ยท GXY Electrode, Cutaneous
ELECTRODE, ELECTROFLEX
| Applicant | Andover Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 27, 1979 |
| Received | Feb 15, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790316
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.