Icad, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Icad, Inc. has 14 FDA 510(k) cleared radiology devices. Based in Beavercreek, US.
Latest FDA clearance: Nov 2024. Active since 2004.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Nov 08, 2024
ProFound Detection (V4.0)
Radiology
269d
Cleared
Jul 12, 2021
PowerLook Density Assessment V4.0
Radiology
59d
Cleared
Mar 12, 2021
ProFound AI Software V3.0
Radiology
73d
Cleared
Oct 04, 2019
ProFound AI Software V2.1
Radiology
70d
Cleared
Dec 06, 2018
PowerLook Tomo Detection V2 Software
Radiology
97d
Cleared
Apr 05, 2018
PowerLook Density Assessment Software
Radiology
79d
Cleared
Feb 25, 2016
Axxent Electronic Brachytherapy System Model 110 XP 1200
Radiology
73d
Cleared
Sep 05, 2014
AXXENT CERVICAL APPLICATOR
Radiology
107d
Cleared
Feb 27, 2013
XOFT AXXENT CERVICAL APPLICATORS
Radiology
111d
Cleared
Jan 17, 2013
XOFT AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM MODEL 110
Radiology
114d
Cleared
Jul 20, 2012
VERSAVUE ENTERPRISE SUITE
Radiology
59d
Cleared
Aug 04, 2010
ICAD VERALOOK CTC CAD SOFTWARE
Radiology
439d
Cleared
Mar 31, 2009
ICAD BREAST INTERVENTIONAL PLANNING SOFTWARE, MODEL D70024
Radiology
60d
Cleared
Nov 19, 2004
SECOND LOOK VIEWER
Radiology
50d