Medical Device Manufacturer · US , Milwaukee , WI

Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc - FDA 510(k) Cleare...

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

Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc has 2 FDA 510(k) cleared medical devices. Based in Milwaukee, US.

Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc
2 devices
1-2 of 2
Cleared Feb 20, 2004
GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587
K040251 · IYN
Radiology · 17d
Cleared Oct 30, 2003
GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X
K032656 · IYN
Radiology · 63d
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