Richard G. Lindsay is one of 6992 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Richard G. Lindsay - FDA 510(k) Cleared Devices
Recent clearances: SWIFT DELIVERY PRODUCT #002-VAC EX CUP W/VAC REL VALVE
1
Total
1
Cleared
0
Denied
Richard G. Lindsay has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Richard G. Lindsay Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Richard G. Lindsay
1 devices