Last synced on 30 September 2022 at 11:05 pm

TENS & EMS Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213835
510(k) Type
Traditional
Applicant
Shenzhen Jian feng Electronic Technology Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/3/2022
Days to Decision
84 days
Submission Type
Summary

TENS & EMS Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213835
510(k) Type
Traditional
Applicant
Shenzhen Jian feng Electronic Technology Co. Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/3/2022
Days to Decision
84 days
Submission Type
Summary