FDA 510(k) Applications Submitted by KIM BLOOM

FDA 510(k) Number Submission Date Device Name Applicant
DEN070014 06/20/2007 MANDOMETER III AB MANDO
K083693 12/12/2008 PB 840 VENTILATOR SYSTEM WITH LEAK COMPENSATION OPTION, MODEL 840 COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT INC.
K063698 12/13/2006 CO2 LASER SYSTEM, MODEL C-LAS CLINICON CORP.


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