510(k) K932202 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)
MODEL 3862A & B 3863A & B TEMP. LEAD SCREENING KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 4, 1994 |
| Received | May 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932202
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.