K242460
- 510(k) number
- K242460
- Device name
- Progenix Select Stim
- Applicant
- Progenix, LLC VA · US
- Product code
- NUH — Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Decision date
- 2025-04-02
- Date received
- 2024-08-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K242460.pdf
Official FDA record: K242460
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.