Lorad, A Hologic Co. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Lorad, A Hologic Co. has 5 FDA 510(k) cleared medical devices. Based in Danbury, US.
Historical record: 5 cleared submissions from 2001 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Lorad, A Hologic Co. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jan 11, 2013
AFFIRM BREAST BIOPSY GUIDANCE SYSTEM
Radiology
116d
Cleared
Jul 05, 2007
DIGITAL STEREOLOC II
Radiology
30d
Cleared
Mar 25, 2003
MULTICARE PLATINUM SYSTEM AND ACCESSORIES
Radiology
22d
Cleared
Oct 24, 2001
MODIFIED 650 MAMMOGRAPHY SYSTEM
Radiology
22d
Cleared
Jul 11, 2001
MODIFIED M-IV MAMMOGRAPHY SYSTEM
Radiology
15d