Nucletron is one of 22052 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nucletron - FDA 510(k) Cleared Devices
Recent clearances: ONCENTRA MANUAL LOW DOSE RATE TREATMENT PLANNING, ONCENTRA PROSTATE 4.0, VAGINAL CT / MR MULTI CHANNEL APPLICATOR SET
3
Total
3
Cleared
0
Denied
Nucletron has 3 FDA 510(k) cleared medical devices. Based in Columbia, US.
Historical record: 3 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Nucletron Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nucletron
3 devices