ELECTRO-GONIOMETER DIAGNOSTIC DEVICE— 510(k) K901290

Name: FDA 510(k) clearance K901290
Creator: U.S. Food and Drug Administration
Published: 1990-10-01

Substantially Equivalent

Chattanooga Group, Inc.

FDA 510(k) clearance K901290 for ELECTRO-GONIOMETER DIAGNOSTIC DEVICE, Substantially Equivalent on 1990-10-01. Applicant: Chattanooga Group, Inc.. Device class: 2.

Clearance details

Applicant: Chattanooga Group, Inc.
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1990-03-20
Decision date: 1990-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hixson, TN, US

Download summary PDF View on FDA.gov ↗

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