510(k) K211971 ยท PZR Percutaneous Nerve Stimulator For Opioid Withdrawal
Drug Relief v1
| Applicant | Dyansys, Inc., San Mateo CA, US |
| Decision | Substantially Equivalent, Nov 5, 2021 |
| Received | Jun 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211971
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.