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FDA 510(k) Applications Submitted by SPAULDING CLINICAL RESEARCH, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150564
03/06/2015
Spaulding Electrocardiograph 2100iQ
Spaulding Clinical Research, LLC
K110065
01/10/2011
SPAULDING IQ ELECTROCARDIOGRAPH
SPAULDING CLINICAL RESEARCH, LLC
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