KIN-COM ASYMMETRICAL BACK SYSTEM— 510(k) K911805

Name: FDA 510(k) clearance K911805
Creator: U.S. Food and Drug Administration
Published: 1991-07-03

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K911805 for KIN-COM ASYMMETRICAL BACK SYSTEM, Substantially Equivalent on 1991-07-03. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1991-04-23
Decision date: 1991-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hixson, TN, US

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