Nucletron Corporation
Nucletron Corporation holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2011.
Top product codes for Nucletron Corporation
Recent clearances by Nucletron Corporation
- K103515 — EQUAL DOSE
- K090706 — ONCENTRA SIMULATION 2.3
- K091154 — UTRECHT INTERSTITIAL FLETCHER CT/MR APPLICATOR SET, MODEL 110.270, INTERSTITIAL RING CT/MR APPLICATOR SET,MODEL 110.330,
- K082642 — ONCENTRA RT VIEWER 1.0
- K080934 — VIENNA RING CT/MR APPLICATOR SET, ROUND POINT TITANIUM NEEDLE SET, TROCAR POINT TITANIUM NEEDLE SET
- K081281 — OCENTRA MASTERPLAN 3.1 (OCENTRA BRACHY)
- K080871 — TROCAR POINT TITANIUM NEEDLE SETS, ROUND POINT TITANIUM NEEDLE SETS
- K080929 — ONCENTRA GYN
- K073273 — EQUAL DOSE 1.0
- K073107 — VALENCIA SKIN APPLICATOR SET, MODEL: 189.701
- K061354 — MICROSELECTRON V3, MODEL 106.990
- K060349 — PROGUIDE NEEDLE SET
- K052228 — SMIT SLEEVE
- K052361 — SIMULIX-EVOLUTION WITH ONCENTRA CONEBEAM
- K033470 — SIMULIX EVOLUTION
- K032372 — NUCLETRON COMFORT CATHETER SYSTEM, MODEL 189.007
- K022739 — REAL TIME HDR (220V), MODEL 132.001; REAL TIME HDR (110V), MODEL 132.002
- K022741 — SPOT PRO (220V), MODEL 131.099
- K022635 — KUSKE BREAST APPLICATOR SET, MODEL 189.006
Data sourced from openFDA. This site is unofficial and independent of the FDA.