FDA 510(k) Applications Submitted by THE SMARTPILL CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K092342 08/04/2009 SMARTPILL GI MONITORING SYSTEM, VERSION 2.0 THE SMARTPILL CORPORATION
K053547 12/20/2005 SMARTPILL GI MONITORING SYSTEM THE SMARTPILL CORPORATION


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