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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