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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