Pie Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pie Medical - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Pie Medical has 12 FDA 510(k) cleared radiology devices. Based in Indianpolis, US.
Historical record: 12 cleared submissions from 2000 to 2006.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pie Medical
12 devices
Cleared
Sep 06, 2006
ART LAB SOFTWARE
Radiology
57d
Cleared
Dec 16, 2005
MYLAB15/20 3D/4D ULTRASOUND IMAGING SYSTEM
Radiology
32d
Cleared
Jan 25, 2005
MYLAB 15 / MYLAB 20, MODEL 2700
Radiology
28d
Cleared
Jan 05, 2005
IMT.LAB
Radiology
29d
Cleared
Jul 23, 2004
PICUS, PARUS, FALCO AND AQUILA ULTRASOUND SYSTEMS
Radiology
32d
Cleared
Dec 15, 2003
TRINGA ULTRASOUND IMAGING SYSTEM, MODEL 50L
Radiology
28d
Cleared
Jan 24, 2003
PICUS ULTRASOUND IMAGING SYSTEMS
Radiology
95d
Cleared
Apr 19, 2002
50S TRINGA ULTRASOUND IMAGING SYSTEM
Radiology
98d
Cleared
Mar 01, 2001
240 PARUS ULTRASOUND IMAGING SYSTEMS, MODEL 240 PARUS
Radiology
87d
Cleared
Jan 05, 2001
260 CORVUS
Radiology
77d
Cleared
Nov 09, 2000
100 S AND 100 LC AND 485 ANSER ULTRASOUND IMAGING SYSTEMS
Radiology
99d
Cleared
Oct 26, 2000
300LC ULTRASOUND IMAGING SYSTEMS, MODEL 300LC
Radiology
41d