George J. Kamilar is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
George J. Kamilar - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
George J. Kamilar has 1 FDA 510(k) cleared medical devices. Based in Brightwaters, US.
Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by George J. Kamilar Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - George J. Kamilar
1 devices