NESS L300— 510(k) K053468

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.

Clearance details

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

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