Medical Device Manufacturer · US , Portland , OR

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

5 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Laerdal Mfg. Corp. has 5 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 5 cleared submissions from 1988 to 1990. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Laerdal Mfg. Corp. Filter by specialty or product code using the sidebar.

Laerdal Mfg. 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 - Laerdal Mfg. Corp.

5 devices

1-5 of 5