MICROWARE 200— 510(k) K050740

Substantially Equivalent

Microware, Inc.

FDA 510(k) clearance K050740 for MICROWARE 200, Substantially Equivalent on 2005-04-06. Applicant: Microware, Inc.. Device class: 2.

Clearance details

Applicant: Microware, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2005-03-22
Decision date: 2005-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vancouver, WA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.