VECTORSONIC, MODEL VU-200— 510(k) K020119

Name: FDA 510(k) clearance K020119
Creator: U.S. Food and Drug Administration
Published: 2002-07-22

Substantially Equivalent

Metron Medical Australia, Pty, Ltd.

FDA 510(k) clearance K020119 for VECTORSONIC, MODEL VU-200, Substantially Equivalent on 2002-07-22. Applicant: Metron Medical Australia, Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Metron Medical Australia, Pty, Ltd.
Product code: Code IMG
Device class: Class 2
Regulation: 21 CFR 890.5860
Advisory panel: Physical Medicine
Date received: 2002-01-14
Decision date: 2002-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carrum Downs, AU

Download summary PDF View on FDA.gov ↗

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