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FDA 510(k) Applications Submitted by MARY CARTER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102426
08/25/2010
CARESCAPE MODEL V100 VITAL SIGNS MONITOR
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
K123996
12/26/2012
RADIAL-CUF NON-INVASIVE BLOOD PRESSURE CUFF
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.
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