William W. Wilkerson & Gregory A. Knutson is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
William W. Wilkerson & Gregory A. Knutson - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
William W. Wilkerson & Gregory A. Knutson has 1 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by William W. Wilkerson & Gregory A. Knutson Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - William W. Wilkerson & Gregory A. Knutson
1 devices