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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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