NESS SYSTEM— 510(k) K022776

Name: FDA 510(k) clearance K022776
Creator: U.S. Food and Drug Administration
Published: 2002-09-11

Substantially Equivalent

Ness-Neuromuscular Electrical Stimulation Systems

FDA 510(k) clearance K022776 for NESS SYSTEM, Substantially Equivalent on 2002-09-11. Applicant: Ness-Neuromuscular Electrical Stimulation Systems. Device class: 2.

Clearance details

Applicant: Ness-Neuromuscular Electrical Stimulation Systems
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2002-08-21
Decision date: 2002-09-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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