K233046
- 510(k) number
- K233046
- Device name
- Electrical Neuromuscular Stimulator, Cure Trio
- Applicant
- Oriental Inspiration Limited CN
- Product code
- GZJ — Stimulator, Nerve, Transcutaneous, For Pain Relief
- Decision date
- 2024-04-19
- Date received
- 2023-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K233046
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.