VECTORSURGE 5, MODEL VS-500— 510(k) K002058

Name: FDA 510(k) clearance K002058
Creator: U.S. Food and Drug Administration
Published: 2001-05-29

Substantially Equivalent

Metron Medical Australia, Pty, Ltd.

FDA 510(k) clearance K002058 for VECTORSURGE 5, MODEL VS-500, Substantially Equivalent on 2001-05-29. Applicant: Metron Medical Australia, Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Metron Medical Australia, Pty, Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2000-07-06
Decision date: 2001-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carrum Downs, AU

Download summary PDF View on FDA.gov ↗

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