K240292
- 510(k) number
- K240292
- Device name
- Transcutaneous Electrical Nerve Stimulator (9029SCM)
- Applicant
- Hong Kong Etech Groups Limited CN
- Product code
- NUH — Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Decision date
- 2024-03-25
- Date received
- 2024-02-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K240292.pdf
Official FDA record: K240292
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.