Nucletron Corporation - FDA 510(k) Cleared Devices
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.
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
Cleared
Nov 09, 2005
SMIT SLEEVE
Radiology
85d
Cleared
Oct 24, 2005
SIMULIX-EVOLUTION WITH ONCENTRA CONEBEAM
Radiology
56d
Cleared
Feb 04, 2004
SIMULIX EVOLUTION
Radiology
93d
Cleared
Aug 15, 2003
NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007
Radiology
14d
Cleared
Oct 25, 2002
REAL TIME HDR (220V), MODEL 132.001
Radiology
67d
Cleared
Oct 24, 2002
SPOT PRO (220V), MODEL 131.099
Radiology
66d
Cleared
Sep 06, 2002
KUSKE BREAST APPLICATOR SET, MODEL 189.006
Radiology
29d