DIGITAL TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL EV-803 DIGITAL TENS— 510(k) K020749

Name: FDA 510(k) clearance K020749
Creator: U.S. Food and Drug Administration
Published: 2002-10-31

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K020749 for DIGITAL TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL EV-803 DIGITAL TENS, Substantially Equivalent on 2002-10-31. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.

Clearance details

Applicant: Everyway Medical Instruments Co.,Ltd
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-03-07
Decision date: 2002-10-31
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

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