Heartlab, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Heartlab, Inc. has 6 FDA 510(k) cleared medical devices. Based in Providence, US.
Historical record: 6 cleared submissions from 1995 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Heartlab, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jun 29, 2005
ASCENTIA HEARTSTATION ECG MANAGEMENT SYSTEM
Cardiovascular
85d
Cleared
Feb 18, 2005
AGFA HEARTLAB CARDIOVASCULAR
Radiology
17d
Cleared
Sep 21, 2004
ULTRASOUND CAPTURE SYSTEM
Radiology
54d
Cleared
Jul 16, 2004
MODIFICATION TO ENCOMPASS
Radiology
101d
Cleared
Feb 21, 1996
DICOMVIEW
Radiology
148d
Cleared
Dec 21, 1995
ECHONET
Radiology
59d