VECTRA PRO MODELS 2 AND 4— 510(k) K982324

Name: FDA 510(k) clearance K982324
Creator: U.S. Food and Drug Administration
Published: 1999-02-01

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K982324 for VECTRA PRO MODELS 2 AND 4, Substantially Equivalent on 1999-02-01. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1998-07-02
Decision date: 1999-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hixson, TN, US

Download summary PDF View on FDA.gov ↗

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