ClearanceBrief
Company ยท US

Ge Medical Systems Ultrasound and Primary Care Dia

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2011. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KGIDensitometer, Bone4
IYNSystem, Imaging, Pulsed Doppler, Ultrasonic2
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 6, 2011K103730GE LUNAR VISCERAL FAT SOFTWARE
Ge Medical Systems Ultrasound and Primary Care Dia
KGI
Nov 21, 2008K072664GE LUNAR FEMUR STRENGTH SOFTWARE
Ge Medical Systems Ultrasound and Primary Care Dia
KGI
Aug 15, 2008K082185GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
Ge Medical Systems Ultrasound and Primary Care Dia
IYO
Dec 19, 2007K073408GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM
Ge Medical Systems Ultrasound and Primary Care Dia
IYN
Sep 14, 2007K072439GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT
Ge Medical Systems Ultrasound and Primary Care Dia
KGI
Oct 20, 2005K052581LUNAR IDXA
Ge Medical Systems Ultrasound and Primary Care Dia
KGI
Jul 23, 2004K041813GE LOGIQ 7 ULTRASOUND BT04
Ge Medical Systems Ultrasound and Primary Care Dia
IYN

Latest recalls

DateFirm and productCodeLinked 510(k)
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