510(k) K810182 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
PROGRAMMABLE SPINAL CORAL STIM. SYSTEM
| Applicant | Electronic Diagnostics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 3, 1981 |
| Received | Jan 22, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810182
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.