Michigan Instruments, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Michigan Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Michigan Instruments, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Feb 14, 2008
THUMPER, MODEL: 1008
Cardiovascular
106d
Cleared
Oct 02, 1997
THUMPER
Cardiovascular
87d
Cleared
Sep 05, 1996
THUMPER CARDIOPULMONARY RESUSCITATOR
Cardiovascular
86d
Cleared
Oct 30, 1989
LARYNGOSTAT LARYNGOSCOPE HANDLE
Anesthesiology
19d
Cleared
May 15, 1985
THUMPER CARDIOPULMONARY RESUSCITATOR 1005
Cardiovascular
55d
Cleared
Dec 27, 1983
CARDIOPULMONARY RESUSCITATOR
Cardiovascular
49d
Cleared
Jul 16, 1981
CARDIOPULMUNARY RESUSCITATOR
Cardiovascular
15d