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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
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