FDA 510(k) Applications Submitted by NUCLETRON CORPORATION
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K091154 |
04/21/2009 |
UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330, |
NUCLETRON CORPORATION |
| K090706 |
03/17/2009 |
ONCENTRA SIMULATION 2.3 |
NUCLETRON CORPORATION |
| K060349 |
02/10/2006 |
PROGUIDE NEEDLE SET |
NUCLETRON CORPORATION |
| K080871 |
03/31/2008 |
TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETS |
NUCLETRON CORPORATION |
| K080929 |
04/01/2008 |
ONCENTRA GYN |
NUCLETRON CORPORATION |
| K080934 |
04/02/2008 |
VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR POINT TITANIUM NEEDLE SET |
NUCLETRON CORPORATION |
| K081281 |
05/06/2008 |
OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY) |
NUCLETRON CORPORATION |
| K061354 |
05/15/2006 |
MICROSELECTRON V3, MODEL 106.990 |
NUCLETRON CORPORATION |
| K032372 |
08/01/2003 |
NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007 |
NUCLETRON CORPORATION |
| K022635 |
08/08/2002 |
KUSKE BREAST APPLICATOR SET, MODEL 189.006 |
NUCLETRON CORPORATION |
| K052228 |
08/16/2005 |
SMIT SLEEVE |
NUCLETRON CORPORATION |
| K022739 |
08/19/2002 |
REAL TIME HDR (220V), MODEL 132.001; REAL TIME HDR (110V), MODEL 132.002 |
NUCLETRON CORPORATION |
| K022741 |
08/19/2002 |
SPOT PRO (220V), MODEL 131.099 |
NUCLETRON CORPORATION |
| K052361 |
08/29/2005 |
SIMULIX-EVOLUTION WITH ONCENTRA CONEBEAM |
NUCLETRON CORPORATION |
| K082642 |
09/11/2008 |
ONCENTRA RT VIEWER 1.0 |
NUCLETRON CORPORATION |
| K033470 |
11/03/2003 |
SIMULIX EVOLUTION |
NUCLETRON CORPORATION |
| K073273 |
11/21/2007 |
EQUAL DOSE 1.0 |
NUCLETRON CORPORATION |
| K073107 |
11/02/2007 |
VALENCIA SKIN APPLICATOR SET, MODEL: 189.701 |
NUCLETRON CORPORATION |
| K103515 |
11/30/2010 |
EQUAL DOSE |
NUCLETRON CORPORATION |
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