Last synced on 25 January 2026 at 3:41 am

ELECTRONIC PULSE STIMULATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131921
510(k) Type
Traditional
Applicant
Shenzhen Jingkehui Electronic Co.., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2013
Days to Decision
142 days
Submission Type
Summary

ELECTRONIC PULSE STIMULATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131921
510(k) Type
Traditional
Applicant
Shenzhen Jingkehui Electronic Co.., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2013
Days to Decision
142 days
Submission Type
Summary