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FDA 510(k) Applications Submitted by MARKUS MARITZ
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970879
03/10/1997
CARDIOVIT CS-200
SCHILLER AMERICA, INC.
K973735
09/30/1997
MICROVIT MT-100
SCHILLER AMERICA, INC.
K973751
10/01/1997
MT-200
SCHILLER AMERICA, INC.
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