MEGVISION, MODEL EQ1000C SERIES— 510(k) K040051

Name: FDA 510(k) clearance K040051
Creator: U.S. Food and Drug Administration
Published: 2004-03-24

Substantially Equivalent

Eagle Technology, Inc.

FDA 510(k) clearance K040051 for MEGVISION, MODEL EQ1000C SERIES, Substantially Equivalent on 2004-03-24. Applicant: Eagle Technology, Inc.. Device class: 2.

Clearance details

Applicant: Eagle Technology, Inc.
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2004-01-12
Decision date: 2004-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Fe, NM, US

Download summary PDF View on FDA.gov ↗

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