Medical Device Manufacturer · US , Washington , DC

Foley & Lardner - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Foley & Lardner has 5 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 5 cleared submissions from 1994 to 1998. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Foley & Lardner Filter by specialty or product code using the sidebar.

Foley & Lardner 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 - Foley & Lardner

5 devices

1-5 of 5