Analogic Corporation - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Analogic Corporation has 7 FDA 510(k) cleared medical devices. Based in Peabody, US.
Last cleared in 2021. Active since 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Analogic Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Analogic Corporation
7 devices
Cleared
Feb 02, 2021
CTxx85 CT Scanner
Radiology
271d
Cleared
Sep 07, 2018
CTXX85
Radiology
30d
Cleared
Feb 13, 2018
CT6485, CT12885
Radiology
222d
Cleared
Jun 15, 2016
Sonic Window
Radiology
33d
Cleared
Mar 04, 2014
SONIC WINDOW
Radiology
47d
Cleared
May 09, 2007
SYNEPIX 4600 DETECTOR
Radiology
44d
Cleared
Dec 27, 2005
FETALGARD LITE-NIBP, MODEL FGL-NIBP
Cardiovascular
167d