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.. Device class: 2.
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
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