510(k) K882887 ยท GXY Electrode, Cutaneous
PROGEL(TM), MODELS 8630 AND 8635
| Applicant | Medical Devices, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Sep 29, 1988 |
| Received | Jul 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882887
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.