FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF PLASTER,FDES107 ABDOMINAL— 510(k) K130723

Name: FDA 510(k) clearance K130723
Creator: U.S. Food and Drug Administration
Published: 2014-02-07

Substantially Equivalent

Famidoc Technology Co., Ltd.

FDA 510(k) clearance K130723 for FDES106 MINI TENS&EMS DEVICE,FDES106 MULTI-FUNCTION MINI TENS&EMS DEVICE,FDES105 PAIN RELIEF PLASTER,FDES107 ABDOMINAL, Substantially Equivalent on 2014-02-07. Applicant: Famidoc Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Famidoc Technology Co., Ltd.
Product code: Code NGX
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2013-03-18
Decision date: 2014-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dongguan, CN

Download summary PDF View on FDA.gov ↗

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