HANDMASTER— 510(k) K031900

Name: FDA 510(k) clearance K031900
Creator: U.S. Food and Drug Administration
Published: 2003-08-08

Substantially Equivalent

Ness-Neuromuscular Electrical Stimulation Systems

FDA 510(k) clearance K031900 for HANDMASTER, Substantially Equivalent on 2003-08-08. 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: 2003-06-19
Decision date: 2003-08-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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