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ELECTRONIC PULSE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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