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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