Igc-Medical Advances, Inc. is one of 14973 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Igc-Medical Advances, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TORSO ARRAY COIL, MODEL 558GE-64
7
Total
7
Cleared
0
Denied
Igc-Medical Advances, Inc. has 7 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 7 cleared submissions from 2000 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Igc-Medical Advances, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Igc-Medical Advances, Inc.
7 devices
Cleared
May 14, 2004
TORSO ARRAY COIL, MODEL 558GE-64
Radiology
8d
Cleared
Mar 22, 2004
MODEL 475 - 8 CHANNEL T/R PHASED ARRAY LOWER EXTREMITY COIL
Radiology
12d
Cleared
Nov 26, 2003
AIRIS-ELITE RAPID BODY COIL, MODEL 554HI-12
Radiology
43d
Cleared
Feb 14, 2003
MODEL 675GE-64 PERIPHERAL VASCULAR COIL CONSISTING OF MODEL 665GE-64: LOWER...
Radiology
87d
Cleared
Dec 22, 2000
MODEL 545PH SERIES: PHASED ARRAY MUSCULO-SKELETAL FLEX COIL
Radiology
53d
Cleared
Jun 20, 2000
MODEL 473SI-64E QUADRATURE LOWER EXTREMITY COIL
Radiology
55d
Cleared
Mar 14, 2000
MODEL 445SI-64E QUADRATURE WRIST COIL
Radiology
21d