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


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