GXW · Class II · 21 CFR 882.1240

FDA Product Code GXW: Echoencephalograph

Leading manufacturers include Storz Instrument Co., Toshiba America Medical Systems, In.C and Hewlett-Packard Co..

7
Total
7
Cleared
126d
Avg days
1977
Since

FDA 510(k) Cleared Echoencephalograph Devices (Product Code GXW)

7 devices
1–7 of 7
Cleared Sep 28, 1992
SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS
K921863
Hewlett-Packard Co.
Radiology · 164d
Cleared Oct 05, 1990
SMS-712NA
K903085
Toshiba America Medical Systems, In.C
Neurology · 85d
Cleared Feb 07, 1986
5.0 IOP & 7.5 IOP PROBES
K853432
Diasonics, Inc.
Neurology · 176d
Cleared May 25, 1984
NEURO SECTOR FIXATION DEVICE
K833522
Advanced Technology Laboratories, Inc.
Neurology · 249d
Cleared Dec 09, 1982
ECHO-PULSE KM555
K821736
Rabar, Inc.
Neurology · 178d
Cleared May 06, 1977
ECHOENCEPHALOGRAPH, DIGITAL,DIGIECHO2000
K770788
Storz Instrument Co.
Neurology · 4d
Cleared Apr 26, 1977
ECHOENCEPHALOGRAPH, DIGITAL, 1000
K770575
Storz Instrument Co.
Neurology · 29d

About Product Code GXW - Regulatory Context