Medical Device Manufacturer · US , Mchenry , IL

Cardiac Resucitator Corp. - FDA 510(k) Cleared Devices

17 submissions · 16 cleared · Since 1981

Total

Cleared

Denied

Cardiac Resucitator Corp. has 16 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1981 to 1988.

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

Cardiac Resucitator 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 - Cardiac Resucitator Corp.

17 devices

1-12 of 17

Cleared Jul 12, 1988

MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR

MODIFIED PACE*AID MODEL 53

K871971 · DRO

Cardiovascular · 34d

Cleared Jun 08, 1987

MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR

PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &

Cardiovascular · 162d

Cardiac Resucitator Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cardiac Resucitator Corp.

Filters