Nucletron Corp. - FDA 510(k) Cleared Devices
Recent clearances: MICROSELECTRON HDR V2, MODEL 105.999, LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS, INTEGRATED BRACHYTHERAPY UNIT - DIGITAL
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nucletron Corp. Radiology ✕
27 devices
Cleared
Oct 08, 2009
MICROSELECTRON HDR V2, MODEL 105.999
Radiology
27d
Cleared
Jun 29, 2009
LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798,...
Radiology
26d
Cleared
Sep 14, 2007
INTEGRATED BRACHYTHERAPY UNIT - DIGITAL
Radiology
15d
Cleared
Mar 24, 2005
INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.001
Radiology
274d
Cleared
Aug 18, 2004
MICROSELECTRON PDR
Radiology
30d
Cleared
Jul 22, 2004
ONCENTRA-VISIR
Radiology
28d
Cleared
Aug 07, 2003
SWIFT 2.0, MODEL 132.001
Radiology
118d
Cleared
Aug 07, 2003
OTP 1.2
Radiology
100d
Cleared
May 23, 2002
MICROSELECTRON HDR- GENIE AFTERLOADING SYSTEM, MODEL 105.989 FOR 115VOLT...
Radiology
30d
Cleared
Mar 13, 2002
IMPLANT GUIDANCE SYSTEM APPLICATOR SET
Radiology
69d
Cleared
Oct 17, 2001
SEED SELECTRON MODEL V. 1.0
Radiology
287d
Cleared
Sep 19, 2001
OLDELFT THORASCAN MODEL NUMBER 180T
Radiology
70d