ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607— 510(k) K033544

Name: FDA 510(k) clearance K033544
Creator: U.S. Food and Drug Administration
Published: 2003-12-10

Substantially Equivalent

Everyway Medical Instruments Co.,Ltd

FDA 510(k) clearance K033544 for ELECTRICAL MUSCLE STIMULATOR, MODELS N605 AND N607, Substantially Equivalent on 2003-12-10. 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: 2003-11-10
Decision date: 2003-12-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

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