DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)— 510(k) K202671

Substantially Equivalent

Guangzhou 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
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.