Last synced on 27 January 2023 at 11:04 pm

Transcutaneous Electrical Nerve Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183288
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/30/2019
Days to Decision
246 days
Submission Type
Summary

Transcutaneous Electrical Nerve Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183288
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/30/2019
Days to Decision
246 days
Submission Type
Summary