Medical Device Manufacturer · US , Portland , OR

Laerdal Mfg. Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Laerdal Mfg. Corp. Cardiovascular ✕

5 devices

1-5 of 5

Cleared Sep 27, 1990

MODIFIED HEARTSTART DEFIBRILLATION ELECTRODE

Cardiovascular · 128d

Cleared Jan 26, 1990

MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODE

Cardiovascular · 14d

Cleared Feb 23, 1989

HEARTSTART 2000 DEFIBRILLATION ELECTRODE

Cardiovascular · 71d

Cleared Sep 12, 1988

HEARTSTART 1000

Cardiovascular · 34d

Cleared Sep 12, 1988

HEARTSTART 1000S

Cardiovascular · 34d