K233166
- 510(k) number
- K233166
- Device name
- NET Recovery Corp/NET Device
- Applicant
- Net Recovery CA · US
- Product code
- PZR — Percutaneous Nerve Stimulator For Opioid Withdrawal
- Decision date
- 2024-05-29
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K233166.pdf
Official FDA record: K233166
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.