FDA 510(k) Applications Submitted by ORSENSE LTD

FDA 510(k) Number Submission Date Device Name Applicant
K142209 08/11/2014 Pulse oximeter NBM-200 ORSENSE LTD
K091564 05/28/2009 NBM-200MP PULSE OXIMETRY DEVICE ORSENSE LTD
K124041 12/28/2012 NBM-200MP ORSENSE LTD


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