Medcom GmbH - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Medcom GmbH has 11 FDA 510(k) cleared radiology devices. Based in Darmstadt, Hessen, DE.
Historical record: 11 cleared submissions from 2002 to 2018.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Sep 21, 2018
VeriSuite
Radiology
78d
Cleared
Mar 27, 2018
Prelude
Radiology
53d
Cleared
Jul 26, 2017
BiopSee, Mobile US
Radiology
127d
Cleared
May 01, 2017
NaviSuite SSI Edition
Radiology
174d
Cleared
Apr 03, 2014
VERISUITE 1.8, VERISUITE-PARTICLE 1.8, VERISUITE, VERISUITE-PARTICLE
Radiology
101d
Cleared
Nov 23, 2010
PVS MODEL 1.0
Radiology
106d
Cleared
May 07, 2010
MEDCOM RT-VIEWER SYSTEM
Radiology
119d
Cleared
Sep 18, 2009
VERISUITE AND VERISUITE-PARTICLE, VERSION 1.8
Radiology
21d
Cleared
May 09, 2008
VERISUITE 1.6, VERISUITE-PARTICLE 1.6
Radiology
53d
Cleared
Sep 25, 2003
EXOMIO, MODEL 2.0 SP1
Radiology
38d
Cleared
Oct 07, 2002
EXOMIO, MODEL 1.1
Radiology
90d