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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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