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FDA 510(k) Applications Submitted by DARIN BUSCH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100121
01/15/2010
MODEL 300157 CPAP SYSTEM
AEIOMED, INC.
K990565
02/22/1999
SUZANNE
NELLCOR PURITAN BENNETT, INC.
K091498
05/20/2009
VITREA ENDOVASCULAR STENT PLANNING SOFTWARE
VITAL IMAGES, INC.
K002001
06/30/2000
BREEZE SLEEPGEAR WITH DREAMSEAL
PURITAN BENNETT CORP.
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