Last synced on 21 June 2024 at 11:04 pm

Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220524
510(k) Type
Traditional
Applicant
Well-Life Healthcare Limited
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/4/2022
Days to Decision
162 days
Submission Type
Summary

Well-Life Mini TENS Stimulator(WL-23XXC/WL-23XXE Series)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220524
510(k) Type
Traditional
Applicant
Well-Life Healthcare Limited
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
8/4/2022
Days to Decision
162 days
Submission Type
Summary