ClearanceBrief
510(k) K090145 ยท OSP Uterine Electromyographic Monitor

SURECALL EMG LABOR MONITOR

ApplicantReproductive Research Technologies, LP, Houston TX, US
DecisionSubstantially Equivalent, Jan 25, 2011
ReceivedJan 21, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090145

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.