Mennen Medical, Inc. - FDA 510(k) Cleared Devices
34
Total
34
Cleared
0
Denied
Mennen Medical, Inc. has 34 FDA 510(k) cleared medical devices. Based in Clarence, US.
Historical record: 34 cleared submissions from 1985 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mennen Medical, Inc. Filter by specialty or product code using the sidebar.
34 devices
Cleared
Feb 26, 2004
ENVOY PATIENT MONITOR
Cardiovascular
356d
Cleared
Oct 08, 1999
ETCO2 VITAL SIGNS MODULE
Anesthesiology
340d
Cleared
Jun 24, 1999
MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS
Cardiovascular
30d
Cleared
Aug 12, 1998
MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR
Cardiovascular
9d
Cleared
Apr 14, 1998
ENVOY PATIENT MONITOR
Cardiovascular
134d
Cleared
Feb 11, 1998
ENSEMBLE CENTRAL STATION MONITOR
Cardiovascular
377d
Cleared
Apr 12, 1995
MERCURY
Cardiovascular
460d
Cleared
Jan 06, 1995
HORIZON 9000 WS
Cardiovascular
343d
Cleared
Mar 23, 1993
CAPNOMED 100 STAND-ALONE ETCO2 MODULE
Anesthesiology
390d
Cleared
Jan 28, 1992
HORIZON 9000/HIS OPTION AMPLIFIER
Cardiovascular
117d
Cleared
Jan 08, 1992
HORIZON PACEMAKER DETECTION SOFTWARE
Cardiovascular
166d
Cleared
Aug 19, 1991
MR-5200 FULL DISCLOSURE SYSTEM
Cardiovascular
151d