KQX · Class I · 21 CFR 888.1500

FDA Product Code KQX: Goniometer, Ac-powered

Leading manufacturers include Orthopedic Systems, Inc., Chattanooga Group, Inc. and Smith & Nephew, Inc..

33
Total
33
Cleared
136d
Avg days
1981
Since

FDA 510(k) Cleared Goniometer, Ac-powered Devices (Product Code KQX)

33 devices
1–24 of 33
Cleared Jul 09, 1997
INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE
K971079
Interlogics, Inc.
Neurology · 106d
Cleared Sep 03, 1996
3D-SPINE
K962377
Skill Technologies, Inc.
Neurology · 75d
Cleared Jun 12, 1996
SPINAL TOUCH
K961212
Fasstech
Neurology · 76d
Cleared Nov 21, 1994
INSIGHT ELECTRONIC ALIGNMENT INDICATOR
K940812
Andronic Devices, Ltd.
Neurology · 272d
Cleared Aug 10, 1992
SPINE MOTION ANALYZER WITH EMG
K920256
Orthopedic Systems, Inc.
Neurology · 202d
Cleared Apr 18, 1990
DYNATRON 360 RANGE OF MOTION TESTING DEVICE
K897178
Dynatronics Corp.
Neurology · 112d
Cleared Jan 19, 1990
COMPREHENSIVE SPINE MOTION ANALYZER
K894283
Orthopedic Systems, Inc.
Neurology · 210d
Cleared Jan 30, 1984
HYPAL ADHESIVE TAPE
K832991
Smith & Nephew, Inc.
Neurology · 150d
Cleared Jul 12, 1983
LAMOREUX-OSI ELECTROGONIOMETER
K831040
Orthopedic Systems, Inc.
Neurology · 103d
Cleared Nov 24, 1981
ELECTRO-GONIOMETER
K812908
Chattanooga Group, Inc.
Neurology · 36d

About Product Code KQX - Regulatory Context