ELECTRONIC PULSE STIMULATOR— 510(k) K131921
Substantially EquivalentShenzhen Jingkehui Electronic Co.., Ltd.
FDA 510(k) clearance K131921 for ELECTRONIC PULSE STIMULATOR, Substantially Equivalent on 2013-11-15. Applicant: Shenzhen Jingkehui Electronic Co.., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Jingkehui 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
- Mountain View, CA, US
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