Mennen Medical , Ltd. - FDA 510(k) Cleared Devices
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
Cleared
Jan 09, 2015
MENNTOR X7
Cardiovascular
221d
Cleared
Dec 27, 2013
CEREBRALOGIK- AEEG
Neurology
192d
Cleared
Aug 30, 2013
HORIZON XVU (FFR)
Cardiovascular
263d
Cleared
May 07, 2010
VITALOGIK 6000/6500
Cardiovascular
151d
Cleared
Aug 07, 2009
HORIZON XVU
Cardiovascular
107d
Cleared
Dec 16, 2008
BIS INTERFACE FOR VITALOGIK PATIENT MONITORS
Neurology
63d
Cleared
Jun 20, 2008
HORIZON XVU
Cardiovascular
23d
Cleared
Nov 21, 2007
VITALOGIK MODEL 4000/4500
Cardiovascular
14d
Cleared
Oct 22, 2007
BIS MODULE FOR ENVOY PATIENT MONITOR
Neurology
105d
Cleared
Sep 07, 2007
EMS-XL CARDIAC ELECTROPHYSIOLOGY SYSTEM
Cardiovascular
116d
Cleared
Apr 19, 2007
HORIZON SE
Cardiovascular
83d
Cleared
Dec 20, 2005
VITALOGIK
Cardiovascular
119d
Cleared
Jan 27, 2005
HORIZON ANGIO CATHLAB
Cardiovascular
31d
Cleared
May 10, 2004
ENVOY PATIENT MONITOR
Neurology
504d
Cleared
Oct 15, 2003
MODIFICATION TO: HORIZON 9000WS
Cardiovascular
20d
Cleared
Dec 03, 2002
MODIFICATION TO ENVOY PATIENT MONITOR
Cardiovascular
19d
Cleared
Aug 01, 2002
ENVOY
Anesthesiology
29d
Cleared
Mar 15, 2002
ENGUARD REMOTE PATIENT MONITOR
Cardiovascular
16d
Cleared
Aug 16, 2001
MODIFICATION TO ENVOY PATIENT MONITOR
Cardiovascular
69d
Cleared
May 08, 2001
ENVOY PATIENT MONITOR
Cardiovascular
396d
Cleared
May 17, 2000
MODIFICATION TO ENVOY PATIENT MONITOR
Cardiovascular
85d