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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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