NESS L300— 510(k) K053468

Name: FDA 510(k) clearance K053468
Creator: U.S. Food and Drug Administration
Published: 2006-07-07

Substantially Equivalent

Ness-Neuromuscular Electrical Stimulation Systems

FDA 510(k) clearance K053468 for NESS L300, Substantially Equivalent on 2006-07-07. Applicant: Ness-Neuromuscular Electrical Stimulation Systems. Device class: 2.

Clearance details

Applicant: Ness-Neuromuscular Electrical Stimulation Systems
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 2005-12-13
Decision date: 2006-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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