Medical Device Manufacturer · US , Menlo Park , CA

Landec Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Landec Corp. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Orthopedic.

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

1 devices

1–1 of 1