Medical Device Manufacturer · IL , Haifa

U.C.G. Technologies , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

U.C.G. Technologies , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Haifa, IL.

Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by U.C.G. Technologies , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - U.C.G. Technologies , Ltd.
2 devices
1-2 of 2
Cleared Jul 18, 2003
MODIFICATION TO WBR, MODEL HR
K031874 · KPS
Radiology · 31d
Cleared Apr 09, 2003
WBR, MODEL HR
K030870 · KPS
Radiology · 21d
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