FDA 510(k) Applications Submitted by MIDWEST REPROCESSING CENTER LLC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K101280	05/06/2010	MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE	MIDWEST REPROCESSING CENTER LLC
K101330	05/12/2010	MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE	MIDWEST REPROCESSING CENTER LLC
K101702	06/17/2010	MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS	MIDWEST REPROCESSING CENTER LLC
K111007	04/11/2011	MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE	MIDWEST REPROCESSING CENTER LLC