FDA 510(k) Applications Submitted by ELAINA COLBY

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
K091598 06/03/2009 LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS NUCLETRON CORP.
K092804 09/11/2009 MICROSELECTRON HDR V2, MODEL 105.999 NUCLETRON CORP.


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