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FDA 510(k) Applications Submitted by COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K092847
09/16/2009
840 VENTILATOR SYSTEM WITH EXPANDED NEOMODE OPTION
COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
K123002
09/27/2012
VITAL SYNC SYSTEM
COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
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.
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