DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)— 510(k) K202671
Substantially EquivalentGuangzhou Xinbo Electronic Co., Ltd.
FDA 510(k) clearance K202671 for DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II), Substantially Equivalent on 2021-11-12. Applicant: Guangzhou Xinbo Electronic Co., Ltd..
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code NUH
- Advisory panel
- Neurology
- 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.