Life Science Instrumentation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Life Science Instrumentation, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Life Science Instrumentation, Inc. has 20 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1981 to 1985.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Life Science Instrumentation, Inc.
20 devices
Cleared
Nov 05, 1985
EMERGIPACE - EXTERNAL PACEMAKER
Cardiovascular
250d
Cleared
Mar 01, 1985
LS 5
Cardiovascular
294d
Cleared
Oct 19, 1984
LS-260G MONITOR/RECORDER & DEFIBILLATOR
Cardiovascular
51d
Cleared
Apr 17, 1984
MINI-DEFIBRILLATOR 280/4
Cardiovascular
96d
Cleared
Apr 28, 1983
VPD540 DEFIBRILLATOR
Cardiovascular
241d
Cleared
Apr 28, 1983
DEFIBRILLATOR VPD 545
Cardiovascular
27d
Cleared
Oct 18, 1982
LS6 ARRYTHMIA DISCRIMINATOR
Cardiovascular
49d
Cleared
Sep 21, 1982
LIFE TRACE 40/42
Cardiovascular
43d
Cleared
Sep 21, 1982
LIFE TRACE 24
Cardiovascular
43d
Cleared
Sep 21, 1982
LIFE WATCH LSI
Cardiovascular
22d
Cleared
Aug 31, 1982
VPD-261 DEFIBRILLATOR MONITOR
Cardiovascular
29d
Cleared
Aug 24, 1982
LIFE TRACE 14
Cardiovascular
15d
Cleared
Jun 17, 1982
CR-9
Cardiovascular
51d
Cleared
Mar 01, 1982
PIONEER II BACK PLATE ELECTRODE
Cardiovascular
42d
Cleared
Sep 25, 1981
CENTERAL MONITOR 360
Cardiovascular
59d
Cleared
Sep 25, 1981
CARDIORATER CR-3
Cardiovascular
59d
Cleared
Sep 25, 1981
CARDIORATER CR-5
Cardiovascular
59d
Cleared
Sep 25, 1981
CARDIORATER CR-7
Cardiovascular
59d
Cleared
Sep 25, 1981
2000 SERIES PORTABLE RESUSCITATION SYST.
Cardiovascular
23d
Cleared
Sep 25, 1981
280/4 MINI-DEFIBRILLATOR
Cardiovascular
23d