DIGITAL ELECTRICAL MUSCLE STIMULATOR, MODEL EV-807 DIGITAL EMS— 510(k) K020750

Name: FDA 510(k) clearance K020750
Creator: U.S. Food and Drug Administration
Published: 2002-10-31

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K020750 for DIGITAL ELECTRICAL MUSCLE STIMULATOR, MODEL EV-807 DIGITAL EMS, 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 IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
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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