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Mennen Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
55
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K141441MENNTOR X7January 9, 2015
K131789CEREBRALOGIK- AEEGDecember 27, 2013
K123792HORIZON XVU (FFR)August 30, 2013
K093766VITALOGIK 6000/6500May 7, 2010
K091165HORIZON XVUAugust 7, 2009
K083063BIS INTERFACE FOR VITALOGIK PATIENT MONITORSDecember 16, 2008
K081484HORIZON XVUJune 20, 2008
K073140VITALOGIK MODEL 4000/4500November 21, 2007
K071899BIS MODULE FOR ENVOY PATIENT MONITOROctober 22, 2007
K071348EMS-XL CARDIAC ELECTROPHYSIOLOGY SYSTEMSeptember 7, 2007
K070254HORIZON SEApril 19, 2007
K052288VITALOGIKDecember 20, 2005
K043564HORIZON ANGIO CATHLABJanuary 27, 2005
K024245ENVOY PATIENT MONITORMay 10, 2004
K030722ENVOY PATIENT MONITORFebruary 26, 2004
K032997MODIFICATION TO: HORIZON 9000WSOctober 15, 2003
K023798MODIFICATION TO ENVOY PATIENT MONITORDecember 3, 2002
K022168ENVOYAugust 1, 2002
K020632ENGUARD REMOTE PATIENT MONITORMarch 15, 2002
K011784MODIFICATION TO ENVOY PATIENT MONITORAugust 16, 2001