FDA 510(k) Applications Submitted by Mia M. Ware

FDA 510(k) Number	Submission Date	Device Name	Applicant
K141542	06/10/2014	NELLCOR PORTABLE SPO2 PATIENT MONITORING SYSTEM ( NPSPMS )	Covidien LLC
K091993	07/02/2009	RAPID PROGRAMMER, VERSION 3.3.0	ADVANCED NEUROMODULATION SYSTEMS, INC. (ANS INC.)
K072462	08/31/2007	WIDE SPACED QUATTRODE LEADS	ADVANCED NEUROMODULATION SYSTEMS
K123581	11/20/2012	NELLCOR OXIMAX N-600X PULSE OXIMETER, NELLCOR BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, NELLCOR BEDSIDE SPO2 PATIEN	COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
K014174	12/20/2001	HARVEY PV DRY STERILIZER, MODEL # ST127325; ST127320; ST127320-33	BARNSTEAD/THERMOLYNE CORP.
K172482	08/16/2017	The Nellcor pulse oximetry monitor interface cable	Covidien