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FDA 510(k) Applications Submitted by SIMUPLAN S.L.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030821
03/14/2003
SIMUPLAN TREATMENT PLANNING SYSTEM, MODEL V. 7.5
SIMUPLAN S.L.
K120551
02/23/2012
SIMUPLAN TREATMENT PLANNING SYSTEM
SIMUPLAN S.L.
K093391
10/30/2009
SIMUPLAN TREATMENT PLANNING SYSTEM
SIMUPLAN S.L.
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