Medical Device Manufacturer · US , Walker , MI

Laerdal California, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1983

Total

Cleared

Denied

Laerdal California, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 5 cleared submissions from 1983 to 1994. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Laerdal California, Inc.

5 devices

1-5 of 5