510(k) K221231 ยท PZR Percutaneous Nerve Stimulator For Opioid Withdrawal
Drug Relief v1
| Applicant | Dyansys, Inc., San Mateo CA, US |
| Decision | Substantially Equivalent, Jun 6, 2022 |
| Received | Apr 29, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K221231
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.