Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)— 510(k) K231789
Substantially EquivalentGuangzhou Xinbo Electronic Co., Ltd.
FDA 510(k) clearance K231789 for Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII), Substantially Equivalent on 2024-03-11. Applicant: Guangzhou Xinbo Electronic Co., Ltd..
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code NGX
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.