Ge Medical Systems F.I. Haifa is one of 474 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Ge Medical Systems F.I. Haifa - FDA 510(k) Cleared Devices
Recent clearances: XELERIS 3.1 PROCESSING AND REVIEW WORKSTATION, XELERIS 3 PROCESSING AND REVIEW WORKSTATION, DISCOVERY MODEL NM/CT 670
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.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Tuv Rheinland of North America, Inc..
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