Medical Device Manufacturer · US , Mchenry , IL

Cook Pacemaker Corp. - FDA 510(k) Cleared Devices

34 submissions · 31 cleared · Since 1981

Total

Cleared

Denied

Cook Pacemaker Corp. has 31 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 31 cleared submissions from 1981 to 1997.

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

Cook Pacemaker Corp. 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 - Cook Pacemaker Corp.

34 devices

1-12 of 34

Cardiovascular · 220d

Cleared Sep 29, 1995

MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS

K953417 · DXY

Cardiovascular · 113d

Cleared Sep 11, 1992

MODEL P IN-LINE BIPOLAR ENDOCARDIAL TINED LEAD

K915188 · DTB

Cardiovascular · 298d

Cleared Oct 16, 1991

MODEL 340 SERIES UNIPOLAR & MODEL 5000B PROGRAMMER

K905403 · DXY

Cardiovascular · 317d

Cleared Oct 08, 1986

MODEL 725TH HANDHELD TRANSCEIVER (PROGRAMMER)

K863582 · DXY

Cardiovascular · 23d

Cleared May 09, 1986

SERIES (T) PROGRAMMABLE CARDIAC PULSE GENERATORS

K861559 · DXY

Cardiovascular · 14d

Cleared Feb 24, 1986

MODEL 327D, SERIES R UNIPOLAR CARDIAC PULSE GENER.

K860202 · DXY

Cardiovascular · 33d

Cleared Feb 24, 1986

MODEL 329D, SERIERS R BIOPOLAR CARDIAC PUL. GEN.

K860466 · DXY

Cardiovascular · 18d

Cleared Dec 19, 1985

BIPOLAR CARDIAC PULSE GENERATOR WITH TELEMETRY

K854919 · DXY

Cardiovascular · 10d

Cleared Dec 03, 1985

COOK PACEMAKER 332T, SERIES R BIPOLAR CARDIAC PULS

K854132 · DXY

Cardiovascular · 54d

Cleared Oct 23, 1985

COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI

K853590 · DXY

Cardiovascular · 56d

Cook Pacemaker Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cook Pacemaker Corp.

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