510(k) K173861 ยท PZR Percutaneous Nerve Stimulator For Opioid Withdrawal
Drug Relief
| Applicant | Dyansys, Inc., San Mateo CA, US |
| Decision | Substantially Equivalent, May 2, 2018 |
| Received | Dec 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173861
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.