Ge Medical Systems F.I. Haifa - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Ge Medical Systems F.I. Haifa has 17 FDA 510(k) cleared radiology devices. Based in Tirat Hacarmel, IL.
Historical record: 17 cleared submissions from 1998 to 2013.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ge Medical Systems F.I. Haifa
17 devices
Cleared
Apr 12, 2013
XELERIS 3.1 PROCESSING AND REVIEW WORKSTATION
Radiology
14d
Cleared
Jan 08, 2010
XELERIS 3 PROCESSING AND REVIEW WORKSTATION
Radiology
15d
Cleared
Dec 10, 2009
DISCOVERY MODEL NM/CT 670
Radiology
27d
Cleared
Dec 12, 2008
GE DISCOVERY NM/CT 570C
Radiology
16d
Cleared
Jan 31, 2008
VENTRI 1.1
Radiology
14d
Cleared
Aug 02, 2005
VENTRI
Radiology
25d
Cleared
Dec 23, 2004
INFINIA LIGHTSPEED
Radiology
14d
Cleared
Dec 30, 2003
MYOLIGHT
Radiology
15d
Cleared
Dec 11, 2002
GE PHOTON ENERGY RECOVERY (PER) OPTION
Radiology
15d
Cleared
Sep 19, 2002
GE QUASAR NUCLEAR MEDICINE SYSTEM
Radiology
13d
Cleared
Dec 21, 2000
QPS/BPGS/MOCO PROCESSING APPLICATIONS FOR ENTEGRA WORKSTATION
Radiology
64d
Cleared
May 03, 2000
EINSTEIN PROCESSING AND REVIEW WORKSTATION
Radiology
86d
Cleared
Mar 07, 2000
CODE AC: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE-ANGLE GAMMA...
Radiology
89d
Cleared
Aug 26, 1999
HAWKEYE OPTION FOR DUAL-HEAD VARIABLE ANGLE GAMMA CAMERA
Radiology
90d
Cleared
Aug 23, 1999
MG ATC: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE-ANGLE GAMMA CAMERA
Radiology
81d
Cleared
Jul 13, 1998
VPC-94 ULTRA HIGH ENERGY COLLIMATERS MODEL NUMBERS 480-685-9402
Radiology
90d
Cleared
Jun 04, 1998
VTRANSACT: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE ANGLE GAMMA...
Radiology
82d