Medical Device Manufacturer · US , Mchenry , IL

Life Sciences Manufacturing, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1979

Total

Cleared

Denied

Life Sciences Manufacturing, Inc. has 12 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1979 to 1991.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Life Sciences Manufacturing, 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 Sciences Manufacturing, Inc.

12 devices

1-12 of 12

Cleared Jul 24, 1991

SFA-II MICROPROCESSOR-CONTROLLED MODULE

K910905 · DRQ

Cardiovascular · 141d

Cleared Jan 16, 1991

IPG-II MODULE

K903700 · DSB

Cardiovascular · 154d

Cleared Jul 18, 1990

CWD/PPG MODULE

K896500 · JOM

Cardiovascular · 246d

Cleared Jul 18, 1990

PAG MICROPROCESSOR-CONTROLLED MODULE

K900365 · DQC

Cardiovascular · 174d

Cleared Mar 27, 1990

PORTABLE AIR PLETHYSMOGRAPH

K895588 · DSB

Cardiovascular · 193d

MVL/MODULAB WITH PVR MODULE

Cardiovascular · 184d

Cleared Jan 03, 1984

NON-INVASIVE CLINICAL VASCULAR LAB

K832679 · DQC

Cardiovascular · 147d

Cleared Sep 28, 1982

CUTANEOUS PRESSURE PLETHYSMOGRAPH

K822522 · DSB

Cardiovascular · 36d

Cleared Jun 18, 1981

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Life Sciences Manufacturing, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Life Sciences Manufacturing, Inc.

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