ClearanceBrief
Company ยท DE

Medcom GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2018. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LHNSystem, Radiation Therapy, Charged-Particle, Medical3
IYEAccelerator, Linear, Medical2
KPQSystem, Simulation, Radiation Therapy2
LLZSystem, Image Processing, Radiological2
MUJSystem, Planning, Radiation Therapy Treatment2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 21, 2018K181789VeriSuite
Medcom GmbH, DE
LHN
Mar 27, 2018K180308Prelude
Medcom GmbH, DE
MUJ
Jul 26, 2017K170841BiopSee, Mobile US
Medcom GmbH, DE
LLZ
May 1, 2017K163119NaviSuite SSI Edition
Medcom GmbH, DE
LLZ
Apr 3, 2014K133914VERISUITE 1.8, VERISUITE-PARTICLE 1.8, VERISUITE, VERISUITE-PARTICLE
Medcom GmbH, DE
LHN
Nov 23, 2010K102237PVS MODEL 1.0
Medcom GmbH, DE
IYE
May 7, 2010K100056MEDCOM RT-VIEWER SYSTEM
Medcom GmbH, DE
MUJ
Sep 18, 2009K092653VERISUITE AND VERISUITE-PARTICLE, VERSION 1.8
Medcom GmbH, DE
LHN
May 9, 2008K080742VERISUITE 1.6, VERISUITE-PARTICLE 1.6
Medcom GmbH, DE
IYE
Sep 25, 2003K032550EXOMIO, MODEL 2.0 SP1
Medcom GmbH, DE
KPQ
Oct 7, 2002K022219EXOMIO, MODEL 1.1
Medcom GmbH, DE
KPQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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