510(k) K200848 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Stimulator, Stimulator Kit, External Transmitter, External Transmitter Kit
| Applicant | Micron Medical Corporation, Boca Raton FL, US |
| Decision | Substantially Equivalent, Aug 14, 2020 |
| Received | Mar 31, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200848
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.