Last synced on 25 April 2025 at 11:05 pm

FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF PLASTER,FDES107 ABDOMINAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130723
510(k) Type
Traditional
Applicant
FAMIDOC TECHNOLOGY CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
326 days
Submission Type
Summary

FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF PLASTER,FDES107 ABDOMINAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130723
510(k) Type
Traditional
Applicant
FAMIDOC TECHNOLOGY CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
326 days
Submission Type
Summary