Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)— 510(k) K190118
Substantially EquivalentGuangzhou Xinbo Electronic Co., Ltd.
FDA 510(k) clearance K190118 for Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III), Substantially Equivalent on 2020-05-13. Applicant: Guangzhou Xinbo Electronic Co., Ltd..
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code GXY
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Panyu, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.