FORTE ES— 510(k) K940759

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K940759 for FORTE ES, Substantially Equivalent on 1995-03-16. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 1994-02-18
Decision date: 1995-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hixson, TN, US

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