Joseph M. Piocentile is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Joseph M. Piocentile - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Joseph M. Piocentile has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1983 to 1983. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Joseph M. Piocentile Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Joseph M. Piocentile
1 devices