ADVANTAGE SIM 6.0— 510(k) K021780

Name: FDA 510(k) clearance K021780
Creator: U.S. Food and Drug Administration
Published: 2002-07-29

Substantially Equivalent

General Electric Medical Systems

FDA 510(k) clearance K021780 for ADVANTAGE SIM 6.0, Substantially Equivalent on 2002-07-29. Applicant: General Electric Medical Systems. Device class: 2.

Clearance details

Applicant: General Electric Medical Systems
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 2002-05-30
Decision date: 2002-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waukesha, WI, US

Download summary PDF View on FDA.gov ↗

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