DUOMED, SERIES 500, (MODELS ID 500, FL 500)— 510(k) K030140

Name: FDA 510(k) clearance K030140
Creator: U.S. Food and Drug Administration
Published: 2003-03-18

Substantially Equivalent

Duomed, Inc.

FDA 510(k) clearance K030140 for DUOMED, SERIES 500, (MODELS ID 500, FL 500), Substantially Equivalent on 2003-03-18. Applicant: Duomed, Inc.. Device class: 2.

Clearance details

Applicant: Duomed, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2003-01-14
Decision date: 2003-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Palm Beach, FL, US

Download summary PDF View on FDA.gov ↗

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