Medical Device Manufacturer · US , Mchenry , IL

Coratomic, Inc. - FDA 510(k) Cleared Devices

15 submissions · 14 cleared · Since 1976

Total

Cleared

Denied

Coratomic, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1976 to 1986.

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

Coratomic, 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 - Coratomic, Inc.

15 devices

1-12 of 15

Cleared Oct 08, 1986

MODIFICATION OF STERILITY CYCLE PARAMETERS

K863365 · DXY

Cardiovascular · 36d

Cleared Dec 15, 1982

CORATOMIC #VX5-105 & VX5-205 PULSE GEN.

CORATOMIC MODEL OVALITH 920BP

K821014 · DXY

Cardiovascular · 46d

Cleared May 28, 1982

CORATOMIC MODEL OVALITH-920

K821033 · DXY

Cardiovascular · 45d

Cleared May 15, 1981

CORATOMIC MODEL OVALITH-920

K810808 · DXY

Cardiovascular · 52d

Cleared Oct 28, 1980

L-15T ENDOCARDIAL PACING ELECTRODE

K802689

Cardiovascular

Cleared Feb 11, 1980

OVALITH P-BP BIPOLAR CARDIAC PACEMAKER

Cardiovascular · 158d

Cleared Dec 04, 1978

OVALITH 10BP

K781377 · DXY

Cardiovascular · 117d

Cleared Jun 14, 1978

L-12, L-21, AND L-22 ELECTRODES

K780569 · DTB

Cardiovascular · 64d

Cleared Feb 06, 1978

ENDOCARDIAL PACING ELECTRODE

K772309 · DTB

Cardiovascular · 59d

Coratomic, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Coratomic, Inc.

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