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FDA 510(k) Applications Submitted by MeVis Medical Solutions AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K201501
06/05/2020
Veolity
MeVis Medical Solutions AG
K120207
01/24/2012
VISIA
MEVIS MEDICAL SOLUTIONS AG
K120484
02/17/2012
VISIA ONCOLOGY
MEVIS MEDICAL SOLUTIONS AG
K113337
11/14/2011
VISIA DYNAMIC REVIEW
MEVIS MEDICAL SOLUTIONS AG
K113701
12/16/2011
VISIA NEURO
MEVIS MEDICAL SOLUTIONS AG
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