510(k) K901809 ยท GXY Electrode, Cutaneous
LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
| Applicant | Lumiscope Co., Inc., Edison NJ, US |
| Decision | Substantially Equivalent, Jun 18, 1990 |
| Received | Apr 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901809
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.