FDA 510(k) Applications Submitted by NUCLETRON

FDA 510(k) Number Submission Date Device Name Applicant
K111973 07/12/2011 VAGINAL CT / MR MULTI CHANNEL APPLICATOR SET NUCLETRON
K112420 08/23/2011 ONCENTRA PROSTATE 4.0 NUCLETRON
K113102 10/19/2011 ONCENTRA MANUAL LOW DOSE RATE TREATMENT PLANNING NUCLETRON


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