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Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162517
510(k) Type
Traditional
Applicant
Jkh Health Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/14/2017
Days to Decision
217 days
Submission Type
Summary

Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162517
510(k) Type
Traditional
Applicant
Jkh Health Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/14/2017
Days to Decision
217 days
Submission Type
Summary