Nucletron Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103515EQUAL DOSESeptember 15, 2011
K090706ONCENTRA SIMULATION 2.3June 15, 2009
K091154UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOMay 18, 2009
K082642ONCENTRA RT VIEWER 1.0November 7, 2008
K080934VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR POINT TITANIUM NEEDLE SETMay 28, 2008
K081281OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)May 20, 2008
K080871TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETSApril 29, 2008
K080929ONCENTRA GYNApril 16, 2008
K073273EQUAL DOSE 1.0December 11, 2007
K073107VALENCIA SKIN APPLICATOR SET, MODEL: 189.701December 7, 2007
K061354MICROSELECTRON V3, MODEL 106.990August 17, 2006
K060349PROGUIDE NEEDLE SETMarch 10, 2006
K052228SMIT SLEEVENovember 9, 2005
K052361SIMULIX-EVOLUTION WITH ONCENTRA CONEBEAMOctober 24, 2005
K033470SIMULIX EVOLUTIONFebruary 4, 2004
K032372NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007August 15, 2003
K022739REAL TIME HDR (220V), MODEL 132.001; REAL TIME HDR (110V), MODEL 132.002October 25, 2002
K022741SPOT PRO (220V), MODEL 131.099October 24, 2002
K022635KUSKE BREAST APPLICATOR SET, MODEL 189.006September 6, 2002