KQW · Class I · 21 CFR 888.1520

FDA Product Code KQW: Goniometer, Nonpowered

Leading manufacturers include Fred Sammons, Inc..

13
Total
13
Cleared
51d
Avg days
1976
Since

FDA 510(k) Cleared Goniometer, Nonpowered Devices (Product Code KQW)

13 devices
1–13 of 13
Cleared Jun 24, 1983
FINGER BONIOMETER BK7506
K831550
Fred Sammons, Inc.
Neurology · 43d
Cleared Feb 27, 1981
UNIVERSAL GONIMETER
K810441
Fred Sammons, Inc.
Neurology · 8d
Cleared Aug 04, 1980
BK-7497 BULB DYNAMOMETER
K801715
Fred Sammons, Inc.
Neurology · 11d
Cleared Aug 04, 1980
BK-7505 RADIOPAQUE GONIOMETER, 8
K801716
Fred Sammons, Inc.
Neurology · 11d
Cleared Aug 04, 1980
BK-7511 BRASS GONIOMETER
K801717
Fred Sammons, Inc.
Neurology · 11d
Cleared Aug 04, 1980
BK-7513 STAINLESS STEEL GONIOMETER
K801718
Fred Sammons, Inc.
Neurology · 11d
Cleared Sep 08, 1976
GONIOMETER, MED. INTER. STAND. BK-7512
K760301
Fred Sammons, Inc.
Neurology · 47d
Cleared Sep 08, 1976
GONIOMETER, INTER. STAND. LARGE, BK7514
K760302
Fred Sammons, Inc.
Neurology · 47d

About Product Code KQW - Regulatory Context