P.T. Kencana Ronasakti Prima is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
P.T. Kencana Ronasakti Prima - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
P.T. Kencana Ronasakti Prima has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by P.T. Kencana Ronasakti Prima Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P.T. Kencana Ronasakti Prima
1 devices