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FDA 510(k) Applications Submitted by SPENCER NEWMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090465
02/23/2009
DIGDOP ULTRASOUND SYSTEM
THE NEWMAN GROUP, LLC
K110628
03/03/2011
SIMPLEABI
NEWMAN MEDICAL
K061091
04/19/2006
BABYBEAT CORDLESS
THE NEWMAN GROUP, LLC
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