NESS CHILDREN SYSTEM— 510(k) K024279

Name: FDA 510(k) clearance K024279
Creator: U.S. Food and Drug Administration
Published: 2003-02-05

Substantially Equivalent

Ness-Neuromuscular Electrical Stimulation Systems

FDA 510(k) clearance K024279 for NESS CHILDREN SYSTEM, Substantially Equivalent on 2003-02-05. Applicant: Ness-Neuromuscular Electrical Stimulation Systems. Device class: 1.

Clearance details

Applicant: Ness-Neuromuscular Electrical Stimulation Systems
Product code: Code IPG
Device class: Class 1
Regulation: 21 CFR 890.3025
Advisory panel: Physical Medicine
Date received: 2002-12-23
Decision date: 2003-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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