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FDA 510(k) Applications Submitted by REPRODUCTIVE RESEARCH TECHNOLOGIES, LP
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130002
01/02/2013
SURECALL LABOR MONITOR
REPRODUCTIVE RESEARCH TECHNOLOGIES, LP
K090145
01/21/2009
SURECALL EMG LABOR MONITOR
REPRODUCTIVE RESEARCH TECHNOLOGIES, LP
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