Kenneth Chapman is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kenneth Chapman - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kenneth Chapman has 1 FDA 510(k) cleared medical devices. Based in Bellaire, US.
Historical record: 1 cleared submissions from 1988 to 1988. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Kenneth Chapman Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kenneth Chapman
1 devices