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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