Life Sensing Instrument Company, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Life Sensing Instrument Company, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Life Sensing Instrument Company, Inc. has 5 FDA 510(k) cleared medical devices. Based in Tullahoma, US.
Historical record: 5 cleared submissions from 1986 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Life Sensing Instrument Company, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Life Sensing Instrument Company, Inc.
5 devices
Cleared
Sep 12, 1997
TELE TRENS TM 10
Cardiovascular
557d
Cleared
Jan 11, 1994
APOLLO CAMERA
Obstetrics & Gynecology
312d
Cleared
Mar 19, 1990
HTS 820 CARDIAC MONITOR
Cardiovascular
91d
Cleared
Apr 10, 1989
HTS 220 CARDIAC MONITOR
Cardiovascular
165d
Cleared
Jun 05, 1986
PARAGON 420, CARDIAC MONITOR
Cardiovascular
77d