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FDA 510(k) Applications Submitted by ELEKTA INC. D/B/A NUCLETRON CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121448
05/15/2012
ONCENTRA, ONCENTRA EXTERNAL BEAM, ONCENTRA BRACHY
ELEKTA INC. D/B/A NUCLETRON CORPORATION
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