Medical Device Manufacturer · US , Washington , DC

King & Spalding - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1994

Total

Cleared

Denied

King & Spalding has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 7 cleared submissions from 1994 to 1995. Primary specialty: General & Plastic Surgery.

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

King & Spalding 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 - King & Spalding

7 devices

1-7 of 7