K241678
- 510(k) number
- K241678
- Device name
- TENS & EMS Stimulator (MHD-1083)
- Applicant
- Shenzhen Minghuangda Electronics Co., Ltd. CN
- Product code
- NUH — Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Decision date
- 2024-09-09
- Date received
- 2024-06-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241678.pdf
Official FDA record: K241678
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.