MAVIDON MEDICAL ELECTRODE JELLY— 510(k) K003924

Name: FDA 510(k) clearance K003924
Creator: U.S. Food and Drug Administration
Published: 2001-08-24

Substantially Equivalent

Mavidon Medical Products

FDA 510(k) clearance K003924 for MAVIDON MEDICAL ELECTRODE JELLY, Substantially Equivalent on 2001-08-24. Applicant: Mavidon Medical Products. Device class: 2.

Clearance details

Applicant: Mavidon Medical Products
Product code: Code GYB
Device class: Class 2
Regulation: 21 CFR 882.1275
Advisory panel: Neurology
Date received: 2000-12-20
Decision date: 2001-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Worth, FL, US

Download summary PDF View on FDA.gov ↗

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