Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Nucletron Corporation

FDA 510(k) & PMA Approved Devices — 19 products

Total Devices19
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K103515 EQUAL DOSEMUJ2011-09-15 View
510(k) K090706 ONCENTRA SIMULATION 2.3KPQ2009-06-15 View
510(k) K091154 UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330,JAQ2009-05-18 View
510(k) K082642 ONCENTRA RT VIEWER 1.0MUJ2008-11-07 View
510(k) K080934 VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR POINT TITANIUM NEEDLE SETJAQ2008-05-28 View
510(k) K081281 OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)MUJ2008-05-20 View
510(k) K080871 TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETSJAQ2008-04-29 View
510(k) K080929 ONCENTRA GYNMUJ2008-04-16 View
510(k) K073273 EQUAL DOSE 1.0IYE2007-12-11 View
510(k) K073107 VALENCIA SKIN APPLICATOR SET, MODEL: 189.701JAQ2007-12-07 View
510(k) K061354 MICROSELECTRON V3, MODEL 106.990JAQ2006-08-17 View
510(k) K060349 PROGUIDE NEEDLE SETJAQ2006-03-10 View
510(k) K052228 SMIT SLEEVEJAQ2005-11-09 View
510(k) K052361 SIMULIX-EVOLUTION WITH ONCENTRA CONEBEAMKPQ2005-10-24 View
510(k) K033470 SIMULIX EVOLUTIONKPQ2004-02-04 View
510(k) K032372 NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007JAQ2003-08-15 View
510(k) K022739 REAL TIME HDR (220V), MODEL 132.001; REAL TIME HDR (110V), MODEL 132.002JAQ2002-10-25 View
510(k) K022741 SPOT PRO (220V), MODEL 131.099MUJ2002-10-24 View
510(k) K022635 KUSKE BREAST APPLICATOR SET, MODEL 189.006JAQ2002-09-06 View
↑