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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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