K231789
- 510(k) number
- K231789
- Device name
- Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd. CN
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2024-03-11
- Date received
- 2023-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K231789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.