Nucletron Corporation is one of 5594 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nucletron Corporation - FDA 510(k) Cleared Devices
Recent clearances: EQUAL DOSE, ONCENTRA SIMULATION 2.3, UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330,
19
Total
19
Cleared
0
Denied
Nucletron Corporation has 19 FDA 510(k) cleared radiology devices. Based in Columbia, US.
Historical record: 19 cleared submissions from 2002 to 2011.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services, Kema Quality B.V. and N.V. Kema.
FDA 510(k) Regulatory Record - Nucletron Corporation
19 devices
Cleared
Sep 15, 2011
EQUAL DOSE
Radiology
289d
Cleared
Jun 15, 2009
ONCENTRA SIMULATION 2.3
Radiology
90d
Cleared
May 18, 2009
UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270,...
Radiology
27d
Cleared
Nov 07, 2008
ONCENTRA RT VIEWER 1.0
Radiology
57d
Cleared
May 28, 2008
VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR...
Radiology
56d
Cleared
May 20, 2008
OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)
Radiology
14d
Cleared
Apr 29, 2008
TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETS
Radiology
29d
Cleared
Apr 16, 2008
ONCENTRA GYN
Radiology
15d
Cleared
Dec 11, 2007
EQUAL DOSE 1.0
Radiology
20d
Cleared
Dec 07, 2007
VALENCIA SKIN APPLICATOR SET, MODEL: 189.701
Radiology
35d
Cleared
Aug 17, 2006
MICROSELECTRON V3, MODEL 106.990
Radiology
94d
Cleared
Mar 10, 2006
PROGUIDE NEEDLE SET
Radiology
28d