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FDA 510(k) Applications Submitted by CHRISTINE DUNN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140959
04/15/2014
ACUSON S1000, S2000, S3000 DIAGNOSTIC ULTRASOUND SYSTEMS
SIEMENS MEDICAL SOLUTIONS USA, INC.
K132804
09/06/2013
ACUSON S1000 / S2000 / S3000
SIEMENS MEDICAL SOLUTIONS USA, INC. ULTRASOUND GRO
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