Medical Device Manufacturer · IL , Rehovot

Mennen Medical , Ltd. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2000
21
Total
21
Cleared
0
Denied

Mennen Medical , Ltd. has 21 FDA 510(k) cleared cardiovascular devices. Based in Rehovot, IL.

Historical record: 21 cleared submissions from 2000 to 2015.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

21 devices
1–12 of 21
MENNTOR X7
K141441 · DSI Detector And Alarm, Arrhythmia · Cardiovascular
Jan 2015 221d
CEREBRALOGIK- AEEG
K131789 · OMA Amplitude-integrated Electroencephalograph · Neurology
Dec 2013 192d
HORIZON XVU (FFR)
K123792 · DQX Wire, Guide, Catheter · Cardiovascular
Aug 2013 263d
VITALOGIK 6000/6500
K093766 · DSI Detector And Alarm, Arrhythmia · Cardiovascular
May 2010 151d
HORIZON XVU
K091165 · DQK Computer, Diagnostic, Programmable · Cardiovascular
Aug 2009 107d
BIS INTERFACE FOR VITALOGIK PATIENT MONITORS
K083063 · OLW Index-generating Electroencephalograph Software · Neurology
Dec 2008 63d
HORIZON XVU
K081484 · DQK Computer, Diagnostic, Programmable · Cardiovascular
Jun 2008 23d
VITALOGIK MODEL 4000/4500
K073140 · DSI Detector And Alarm, Arrhythmia · Cardiovascular
Nov 2007 14d
BIS MODULE FOR ENVOY PATIENT MONITOR
K071899 · OLW Index-generating Electroencephalograph Software · Neurology
Oct 2007 105d
EMS-XL CARDIAC ELECTROPHYSIOLOGY SYSTEM
K071348 · DQK Computer, Diagnostic, Programmable · Cardiovascular
Sep 2007 116d
HORIZON SE
K070254 · DQK Computer, Diagnostic, Programmable · Cardiovascular
Apr 2007 83d
VITALOGIK
K052288 · DSI Detector And Alarm, Arrhythmia · Cardiovascular
Dec 2005 119d
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