Medical Device Manufacturer · US , Mchenry , IL

Life Science Instrumentation, Inc. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1981

Total

Cleared

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.

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.

FDA 510(k) Regulatory Record - Life Science Instrumentation, Inc.

20 devices

1-12 of 20

Cleared Nov 05, 1985

EMERGIPACE - EXTERNAL PACEMAKER

K850812 · DRO

Cardiovascular · 250d

Cleared Mar 01, 1985

LS 5

K842037 · DRT

Cardiovascular · 294d

Cleared Oct 19, 1984

LS-260G MONITOR/RECORDER & DEFIBILLATOR

K843396 · LDD

Cardiovascular · 51d

Cleared Apr 17, 1984

MINI-DEFIBRILLATOR 280/4

Cardiovascular · 241d

Cleared Apr 28, 1983

DEFIBRILLATOR VPD 545

K831056 · LDD

Cardiovascular · 27d

Cleared Oct 18, 1982

LS6 ARRYTHMIA DISCRIMINATOR

VPD-261 DEFIBRILLATOR MONITOR

Life Science Instrumentation, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Life Science Instrumentation, Inc.

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